Category: nitriles-buliding-blocks

Application of 3759-28-2, As we all know, there are many different methods for the synthesis of a compound, and people can choose the synthesis method that suits their own laboratory according to the actual situation. 3759-28-2 name is 2-(Cyanomethyl)benzonitrile, This compound is widely used in many fields, so it is necessary to find a new synthetic route. The downstream synthesis method of this compound is introduced below.

General procedure: A mixture of each of 1 (2.38 g, 0.01 mol) and appropriate nitriles 2a-d (0.01 mol) in the presence ofammonium acetate (1.54 g, 0.02 mol) was heated in an oil-bath at 150 oC for 45 min. The reaction mixturewas poured onto ice/HCl. The solid that separated out was filtered, dried and recrystallized fromEtOH-DMF to give compounds 3a-d.

At the same time, in my other blogs, there are other synthetic methods of this type of compound, 2-(Cyanomethyl)benzonitrile, and friends who are interested can also refer to it.

Reference:
Article; Fadda, Ahmed A.; Mohamed, Khaled S.; Refat, Hala M.; El-Bialy, Engy E.; Heterocycles; vol. 91; 1; (2015); p. 134 – 148;,
Nitrile – Wikipedia,
Nitriles – Chemistry LibreTexts

Application of 403-54-3,Some common heterocyclic compound, 403-54-3, name is 3-Fluorobenzonitrile, molecular formula is C7H4FN, traditional synthetic route has been very mature, but the traditional synthetic route has various shortcomings, such as complicated route, low yield, poor purity, etc, below Introduce a new synthetic route.

General procedure: Benzonitrile 1a (1 mmol), Na2S*9H2O (1.2 mmol) and DMF (1 mL) were added into a 10 mL bottle. The reactor was placed in a heating magnetic stirrer at 130 C. After 2.5 h, by adding about 3 mL H2O after the reaction to disperse the solid product, the reaction mixture was extracted with EtOAc (3 x 3 mL), and the mixture was purified by column chromatography.

The synthetic route of 403-54-3 has been constantly updated, and we look forward to future research findings.

Reference:
Article; Cao, Xian Ting; Yang, Huiyong; Zheng, Hui; Zhang, Pengfei; Heterocycles; vol. 96; 3; (2018); p. 509 – 517;,
Nitrile – Wikipedia,
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Related Products of 21423-81-4,Some common heterocyclic compound, 21423-81-4, name is 3-Chloro-4-methylbenzonitrile, molecular formula is C8H6ClN, traditional synthetic route has been very mature, but the traditional synthetic route has various shortcomings, such as complicated route, low yield, poor purity, etc, below Introduce a new synthetic route.

Example 53 3- {5-[4-(6-Methoxy-pyridin-3-yl)-5-methyl-4H-[1,2,4]triazol-3-yl]-pyra zin-2-yl} -4-methyl-benzonitrile A mixture of 3-chloro-4-methylbenzonitrile (1g, 6. 6mmol), bis (PINACOLATO) DIBORON (1. 8G,. 7. 0MMOL), caesium carbonate (6. 4g, 19. 8MMOI) and the product of . preparation 3 (5mg, cat) in 1,4-dioxan (50mL) was heated under reflux for 4 hours. The reaction mixture was then cooled TO ROOM TEMPERATURE, FILTERED through CELITENo. AND CONCENTRATED IN VACUO. A portion of the residue (145mg, 0. 6MMOL), the product of preparation 30 (90MG, 0. 3MMOL), caesium carbonate (293mg, 0. 9mmol) and the product of preparation 3 (2mg, cat) were then dissolved in 1,4-dioxan and the mixture was heated under reflux for 18 hours. The mixture was then cooled to room temperature, filtered through Celiez and concentrated IN VACUO. Purification of the residue by . column chromatography on silica gel, eluting with dichloromethane : methanol, 100: 0 to 97: 3, afforded the title compound as a white solid in 3% yield, 3mg. HNMR (CDCl3, 400MHZ) 5 : 2.41 (s, 3H), 2.46 (s, 3H), 4.02 (s, 3H), 6.90 (d, 1H), 7.43 (d, 1H), 7.53 (DD, 1H), 7.63 (dd, 1H), 7. 70 (d, 1H), 8. 09 (d, 1H), 8.41 (d, 1H), 9. 55 (D, 1 H). MS APCI+ m/z 383 [MH] +

These compound has a wide range of applications. It is believed that with the continuous development of the source of the synthetic route 3-Chloro-4-methylbenzonitrile, its application will become more common.

Reference:
Patent; PFIZER LIMITED; PFIZER INC.; WO2005/28452; (2005); A1;,
Nitrile – Wikipedia,
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Related Products of 140860-51-1,Some common heterocyclic compound, 140860-51-1, name is 2-Bromo-4-methoxybenzonitrile, molecular formula is C8H6BrNO, traditional synthetic route has been very mature, but the traditional synthetic route has various shortcomings, such as complicated route, low yield, poor purity, etc, below Introduce a new synthetic route.

Step b. To a stirred solution of tert-butyl 6-(methylsulfonamido)-4-(4,4,5,5-tetramethyl-l,3,2- dioxaborolan-2-yl)isoindoline-2-carboxylate (1.030 g, 2.37 mmol) in l,4-dioxane:water (9: 1, 5 ml) were added K2C03 (0.300 g, 2.37 mmol) and 2-bromo-4-methoxybenzonitrile (CAS Number 140860- 51-1; 0.250 g, 1.185 mmol) at rt. The reaction mixture was degassed for 20 min before addition of PdCl2(dppf) (0.087 g, 0.118 mmol). The resulting reaction mixture was heated at 90C for 2 h. The reaction mixture was cooled to rt, poured into water (50 ml) and extracted with EtOAc (2 x 50 ml). The combined organic phase washed with brine (40 ml), dried over Na2S04, filtered and concentrated under reduced pressure. The residue was purified by flash column chromatography (8 % EtOAc in hexane) yielding tert-butyl 4-(2-cyano-5-methoxyphenyl)-6-(methylsulfonamido)isoindoline-2- carboxylate (0.150 g, 0.338 mmol). LCMS: Method A, 2.038 min, MS: ES+ 444.6; NMR (400 MHz, DMSO-d6) delta ppm 9.99 (s, 1H), 7.89 (t, J= 6.0 Hz, 1H), 7.23 – 7.10 (m, 4 H), 4.64 (d, J=11.2, 2 H), 4.42 (d, J=10.4, 2 H), 3.85 (s, 3 H), 3.02 (s, 3 H), 1.40 (d, J=15.6 Hz, 9 H).

The synthetic route of 140860-51-1 has been constantly updated, and we look forward to future research findings.

Reference:
Patent; MISSION THERAPEUTICS LIMITED; GIBSON, Karl Richard; JONES, Alison; KEMP, Mark Ian; MADIN, Andrew; STOCKLEY, Martin Lee; WHITLOCK, Gavin Alistair; WOODROW, Michael D; (241 pag.)WO2017/158388; (2017); A1;,
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Synthetic Route of 78473-00-4, The chemical industry reduces the impact on the environment during synthesis 78473-00-4, name is 4-Amino-3,5-dichlorobenzonitrile, I believe this compound will play a more active role in future production and life.

EXAMPLE 21 7-Difluoromethoxy-2-ethylfuro[2,3-c]pyridine-4-carboxylic acid (2,6-dichloro-4-cyanophenyl)amide Starting from 7-difluromethoxy-2-ethylfuro[2,3-c]pyridine-4-carboxylic acid 4-nitrophenyl ester (100 mg) and 4-amino-3,5-dichlorobenzonitrile (99 mg). Purification by column chromatography on silica eluding with 1% methanol in dichloromethane afforded the title compound as a white solid (12 mg). TLC Rf 0.65 (2.5% methanol in dichloromethane) m.p. 208-210 C.

In the field of chemistry, the synthetic routes of compounds are constantly being developed and updated. I will also mention this compound in other articles, 4-Amino-3,5-dichlorobenzonitrile, other downstream synthetic routes, hurry up and to see.

Reference:
Patent; Darwin Discovery, Ltd.; US6169090; (2001); A;,
Nitrile – Wikipedia,
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Some common heterocyclic compound, 38487-86-4, name is 2-Amino-4-chlorobenzonitrile, molecular formula is C7H5ClN2, traditional synthetic route has been very mature, but the traditional synthetic route has various shortcomings, such as complicated route, low yield, poor purity, etc, below Introduce a new synthetic route. SDS of cas: 38487-86-4

Method 2 (from 3-ethylacetate-2-oxa-l-adamantyl methanesulfonate (3))A suspension of anhydrous A1C13 (417 mg, 3.13 mmol) and mesylate (3) (830 mg, 2.6 mmol) in dry 1 ,2-dichloroethane (4 mL) was stirred at reflux. The reaction mixture became orange and exothermic. After 5 minutes, a suspension of 4-chloro-2-aminobenzonitrile (438 mg, 2.87 mmol) in dry 1 ,2-dichloroethane (5 mL) was added dropwise to the refluxing mixture and the reflux was maintained for 8h. The reaction mixture was then cooled to r. , diluted with water (10 mL) and THF (10 mL), basified by addition of 5 M NaOH solution (10 mL) and stirred at r.t. for 30 min. The phases were separated (DCM was added if necessary) and the aqueous layer was extracted with AcOEt (3 x 20 mL). The combined organic layers were dried with Na2S04 and concentrated under reduced pressure to afford a yellow solid. Purification by flash chromatography (cyclohexane / AcOEt 10/0 to AcOEt / MeOH 9/1, v/v) afforded a pale yellow solid. Recrystallisation from petroleum ether / AcOEt, 8/2, v/v afforded the desired Huprine (HUP 1) as a white solid (799 mg, 88%).Rf (AcOEt / MeOH 9/1, v/v) = 0.33.m.p. = 179-180C.IR (KBr): v = 3352, 3209, 2929, 1727, 1648, 1609 ,1559, 1490, 1426, 1371, 1308, 1285, 1258, 1154, 1031, 929 cm”1.1H NMR (300 MHz, CDC13): delta = 0.99 (t, J = 7.2 Hz, 3H, ¾), 1.88-1.93 (m, 1H, H10), 2.02-2.08 (m, 2H, ¾<>, ¾), 2.57 (dd, J = 17.1 Hz, J = 3.9 Hz, 1H, ¾), 2.70-2.74 (m, 1H, H7), 2.72-2.77 (m, 2H, ¾), 2.94 (d, J= 17.7 Hz, 1H, H6), 3.11 (dd, J= 17.5 Hz, J = 5.5 Hz, 1H, H6), 3.16-3.20 (m, 1H, H?), 3.92 (q, J = 7.1 Hz, 2H, Hi7), 5.05 (brs, 2H, NH2), 5.67 (d, J= 5.1 Hz, 1H, H8), 7.21 (dd, J= 9.0 Hz, J = 1.9 Hz, 1H, H2), 7.65 (d, J= 9.0 Hz, 1H, Hi), 7.81 (d, J= 1.9 Hz, 1H, H4).13C NMR (75 MHz, CDC13): delta = 14.0 (Ci8), 27.4 (Cn), 28.4 (C7), 28.8 (C10), 33.9 (C13), 39.2 (C6), 43.3 (CM), 60.6 (C17), 114.9 (Cl la or C12a), 115.8 (Cl la or C12a), 121.9 (Ci), 124.7 (C2), 127.1 (C4), 129.5 (C8), 129.8 (C9), 134.6 (C3), 146.4 (C4a or C12), 146.9 (C4aor C12), 158.1 (C5a), 171.5 (C15).MS (ESI+): m/z (%): 357.33 (100) [M+H]+, 359.20 (36). ICso rh-AC E : 3.90 +/- 0.50 iiM.ICso r/i-BuChE : 137 +/- 1 1 iiM.ICso erythrocyte /i-AChE : 38.3 iiM.

These compound has a wide range of applications. It is believed that with the continuous development of the source of the synthetic route 38487-86-4, its application will become more common.

Reference:
Patent; UNIVERSITE DE ROUEN; RONCO, Cyril; RENARD, Pierre Yves; JEAN, Ludovic; NACHON, Florian; ROMIEU, Anthony; WO2011/124712; (2011); A1;,
Nitrile – Wikipedia,
Nitriles – Chemistry LibreTexts

Related Products of 10412-93-8, As we all know, there are many different methods for the synthesis of a compound, and people can choose the synthesis method that suits their own laboratory according to the actual situation. 10412-93-8 name is N-Benzyl-2-cyanoacetamide, This compound is widely used in many fields, so it is necessary to find a new synthetic route. The downstream synthesis method of this compound is introduced below.

General procedure: (E)–aryl–cyanoacrylamides 2 was prepared according to literature procedure.2 General procedure for 2a. To a solution of benzaldehyde (10 mmol 1.0 equiv), pyrrolidine (2 mmol, 20 mol %) in ethanol (20 mL) was added N-benzyl-2-cyanoacetamide (10 mmol, 1.0 equiv). The reaction mixture was stirred at room temperature until the reaction was complete (monitored by TLC), the solvent was removed under reduced pressure. The crude reaction mixture was purified through flash column chromatography on silica gel to afford 2a.

At the same time, in my other blogs, there are other synthetic methods of this type of compound, N-Benzyl-2-cyanoacetamide, and friends who are interested can also refer to it.

Reference:
Article; Nie, Xufeng; Wang, Yachuan; Yang, Lijun; Yang, Zaijun; Kang, Tairan; Tetrahedron Letters; vol. 58; 31; (2017); p. 3003 – 3007;,
Nitrile – Wikipedia,
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Researchers who often do experiments know that organic synthesis is a process of preparing more complex target molecules from simple raw materials through one or more chemical reactions. Generally, it requires fewer steps, and cheap raw materials. 3218-50-6, name is 2,5-Dichlorobenzyl cyanide, A new synthetic method of this compound is introduced below., COA of Formula: C8H5Cl2N

To a stirred solution of 2-(2,5-dichlorophenyl)acetonitrile (700 mg, 3.76 mmol, 1.00 equiv) in water (6 mL) was added sulfuric acid (8 mL) dropwise. The resulting solution was stirred for 3 h at 110 C in an oil bath, diluted with H20 (100 mL), extracted with dichloromethane (3×50 mL) and the combined organic layers washed with brine (3×100 mL), dried over anhydrous sodium sulfate and concentrated under reduced pressure to provide 700 mg (91%) of the product as a white solid.

The basis of chemical reaction formula synthesis, the synthesis route is composed of some specific reactions and combined according to certain logical thinking. We look forward to the emergence of more reaction modes in the future.

Reference:
Patent; ARDELYX, INC.; LEWIS, Jason, G.; REICH, Nicholas; CHEN, Tao; JACOBS, Jeffrey W.; CHARMOT, Dominique; NAVRE, Marc; FINN, Patricia; CARRERAS, Christopher; SPENCER, Andrew; WO2013/96771; (2013); A1;,
Nitrile – Wikipedia,
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Electric Literature of 90110-98-8,Some common heterocyclic compound, 90110-98-8, name is 3-Bromo-4-(hydroxymethyl)benzonitrile, molecular formula is C8H6BrNO, traditional synthetic route has been very mature, but the traditional synthetic route has various shortcomings, such as complicated route, low yield, poor purity, etc, below Introduce a new synthetic route.

LiAlH4 (34.0 mmol; 34.0 mL of a 1.0 M solution in THF) was cooled to 0 C using an ice bath then treated with MeOH (102 mmol; 26.4 mL of a 3.86 M solution in THF) dropwise over 5 min. The product of Part 3C (0.900 g, 4.24 mmol) was then added and the resulting solution warmed slowly to ambient temperature as the ice bath melted. After 16 h total reaction time, the solution was diluted with H2O (9.0 mL) and the resulting suspension filtered through a scintered glass funnel of medium porosity. The solids were exhaustively washed with H2O and Et2O then transferred to a separatory funnel and split. The aqueous layer was further washed with Et2O and EtOAc and the combined organic layers dried over Na2SO4, filtered and concentrated in vacuo to a yellow solid (0.591 g), which was used without further purification in the subsequent reaction.

These compound has a wide range of applications. It is believed that with the continuous development of the source of the synthetic route 3-Bromo-4-(hydroxymethyl)benzonitrile, its application will become more common.

Reference:
Patent; LANTHEUS MEDICAL IMAGING, INC.; RADEKE, Heike, S.; CESATI, Richard, R.; PUROHIT, Ajay; HARRIS, Thomas, D.; ROBINSON, Simon, P.; YU, Ming; CASEBIER, David, S.; HU, Carol, Hui; BROEKEMA, Matthias; ONTHANK, David, C.; WO2013/36869; (2013); A2;,
Nitrile – Wikipedia,
Nitriles – Chemistry LibreTexts

Related Products of 5332-06-9, These common heterocyclic compound, 5332-06-9, name is 4-Bromobutanenitrile, its traditional synthetic route has been very mature, but the traditional synthetic route has various shortcomings, such as complicated route, low yield, poor purity, etc, below Introduce a new synthetic route.

(trans) 1-(1 H-benzimidazol-2-ylmethyl)-2,3,3a,4,5,9b-hexahydro-1 H-pyrrolo[3,2- /?]quinoline (0.032 g, 0.11 mmol), potassium carbonate (0.075 g, 0.55 mmol), 4- bromobutanenitrile (0.024 g, 0.16 mmol), and potassium iodide (5 mg) in 3 ml_ of N,N-dimethyIformamide were heated to 80 2C in a sealed tube for 16 hours. The mixture was allowed to cool to room temperature and quenched with 5 ml_ of water. The mixture was extracted 3 times with 5 mL of dichloromethane and the combined organic layers concentrated. The residue was dissolved in 20 mL of a 2M ammonia solution in methanol and hydrogenated under 40 psi of hydrogen for 18 hours, with 30 mg of raney nickel as catalyst. The catalyst was filtered off over celite and the filtrate concentrated. The residue was purified by silica chromatography eluting with a 0% to 10% gradient of aqueous ammonia in acetonitrile to yield 29 mg (70%) of (trans) 4-[2-(2,3,3a,4,5,9b-hexahydro-1 H-pyrrolo[3,2-/7]quinolin-1 -ylmethyl)-1 H- benzimidazol-1-yl]-1 -butanamine. 1 H NMR (400 MHz, METHANOL-D4) delta ppm 1.1 (m, 2 H), 1.4 (m, 2 H), 1.7 (m, 2 H), 1.8 (m, 1 H), 2.1 (m, 1 H), 2.4 (m, 1 H), 2.5 (t, J=7.4 Hz, 2 H), 2.7 (m, 1 H), 2.8 (m, 2 H), 2.9 (m, 1 H), 3.6 (d, J=8.6 Hz, 1 H), 3.6 (d, J=13.6 Hz, 1 H), 3.7 (m, 1 H), 3.8 (m, 1 H), 4.7 (d, J=13.6 Hz, 1 H), 7.2 (m, 2 H), 7.4 (m, 2 H), 7.6 (m, 1 H), 7.7 (d, J=7.9 Hz, 1 H), 8.4 (d, J=6.4 Hz, 1 H); MS m/z376(M+1).

The synthetic route of 5332-06-9 has been constantly updated, and we look forward to future research findings.

Reference:
Patent; SMITHKLINE BEECHAM CORPORATION; WO2006/96444; (2006); A2;,
Nitrile – Wikipedia,
Nitriles – Chemistry LibreTexts