Tag: 100-200

On January 25, 1990, Yoshikawa, Yoshinari; Ochi, Yutaka; Sekiuchi, Kazuto; Saito, Hideji; Hatayama, Katsuo published a patent.HPLC of Formula: 34662-29-8 The title of the patent was Preparation of sulfonanilide derivatives as antiinflammatory agents. And the patent contained the following:

Sulfonanilides [I; R1 = C1-4 alkyl; R2 = C1-4 alkyl, Ph, AR4 wherein R4 = Ph, halo-substituted Ph or cycloalkyl, A = O, S; R3 = halo, haloalkyl, Ph, CHO, alkoxycarbonyl, etc.] are prepared Reduction of 5.0 g nitro compound II (R = NO2) in EtOH over 5% Pd-C gave 4.4 g amine II (R = NH2), which (3.3 g) was diazotized and the diazonium salt treated with KCN to give 1.2 g cyano compound II (R = cyano) (III). III at 50 mg/kg p.o. showed 48.9% inhibition of carrageenan-induced edema in rats, vs. 41.6% inhibition with ibuprofen. Also prepared were 35 addnl. I. The experimental process involved the reaction of 3-Chloro-4-nitrobenzonitrile(cas: 34662-29-8).HPLC of Formula: 34662-29-8

The Article related to sulfonanilide preparation antiinflammatory, Benzene, Its Derivatives, and Condensed Benzenoid Compounds: Amides, Amidines, Imidic Esters, Hydrazides, and Hydrazonic Esters and other aspects.HPLC of Formula: 34662-29-8

Referemce:
Nitrile – Wikipedia,
Nitriles – Chemistry LibreTexts

On December 1, 2021, Desai, Jigar; Patel, Bhaumin; Darji, Brijesh; Gite, Archana; Panchal, Nandini; Bhosale, Gokul; Shedage, Sandeep; Patel, Sandip; Kadam, Pravin; Patel, Gautam; Kumar Srivastava, Brijesh; Joharapurkar, Amit; Kshirsagar, Samadhan; Giri, Poonam; Bhayani, Hitesh; Patel, Ankit; Ghoshdastidar, Krishnarup; Bandyopadhyay, Debdutta; Kumar, Sanjay; Jain, Mukul; Sharma, Rajiv published an article.Quality Control of 3-Chloro-4-nitrobenzonitrile The title of the article was Discovery of novel, potent and orally efficacious inhibitor of neutral amino acid transporter B0AT1 (SLC6A19). And the article contained the following:

Rationally designed trifluoromethylsulfonyl derivatives were identified as novel, potent and orally bioavailable B0AT1 (neutral amino acid transporter) inhibitors. The compound I was found to be nanomolar potent (IC50: 0.035渭M) B0AT1 inhibitor with excellent pharmacokinetic profile (%F: 66) in mice and efficacious in vivo in diet induced obese (DIO) mice model. The experimental process involved the reaction of 3-Chloro-4-nitrobenzonitrile(cas: 34662-29-8).Quality Control of 3-Chloro-4-nitrobenzonitrile

The Article related to aryl sulfonamide preparation b0at1 neutral amino acid transporter inhibitor, b(0)at1, nimesulide, nitro group, trifluoromethyl sulfonyl, Benzene, Its Derivatives, and Condensed Benzenoid Compounds: Sulfenic, Sulfinic, and Sulfonic Acids and Derivatives and other aspects.Quality Control of 3-Chloro-4-nitrobenzonitrile

Referemce:
Nitrile – Wikipedia,
Nitriles – Chemistry LibreTexts

On September 25, 1992, Tsuji, Kiyoshi; Nakamura, Katsuya; Konishi, Nobukiyo; Okumura, Hiroyuki; Matsuo, Masaaki published an article.Safety of 3-Chloro-4-nitrobenzonitrile The title of the article was Studies on antiinflammatory agents. I. Synthesis and pharmacological properties of 2′-phenoxymethanesulfonanilide derivatives. And the article contained the following:

Various 2′-phenoxymethanesulfonanilide derivatives I (R1 = H, NO2, CF3, CONH2, SEt, cyano, etc., R2 = H, COMe, Me) and II (R3-R5 = H, 2-F, 2,3-Cl2, 2-Br, 2-OMe, 2-SMe, etc.) were synthesized and evaluated for antiinflammatory and analgesic activities. Thus, 3-(2,4-difluorophenoxy)-4-nitrobenzonitrile reacted with Fe/NH4Cl/EtOH and MeSO2Cl/pyridine to give I (R1 = cyano, R2 = H). Some compounds bearing an electron-attracting substituent at the 4′-position strongly inhibited adjuvant-induced arthritis in rats and acetic acid-induced writhing syndrome in mice without causing gastro-intestinal irritation. Among them, 4′-cyano-(FK867) and 4′-acetyl-(FK3311) 2′-(2,4-difluorophenoxy)methanesulfonanilides were selected as the candidates for further development. The experimental process involved the reaction of 3-Chloro-4-nitrobenzonitrile(cas: 34662-29-8).Safety of 3-Chloro-4-nitrobenzonitrile

The Article related to phenoxymethanesulfonanilide preparation analgesic antiinflammatory, Benzene, Its Derivatives, and Condensed Benzenoid Compounds: Sulfenic, Sulfinic, and Sulfonic Acids and Derivatives and other aspects.Safety of 3-Chloro-4-nitrobenzonitrile

Referemce:
Nitrile – Wikipedia,
Nitriles – Chemistry LibreTexts

On November 30, 1988, Matsuo, Masaaki; Tsuji, Kiyoshi; Konishi, Nobukiyo; Okumura, Hiroyuki published a patent.Application In Synthesis of 3-Chloro-4-nitrobenzonitrile The title of the patent was Preparation of alkanesulfonanilides as analgesics and antiinflammatories. And the patent contained the following:

The title compounds [I; Ar = Q; R1 = alkyl, haloalkyl; R2 = acyl, cyano, CO2H, (un)substituted alkyl, etc.; R3 = H, NO2, alkyl, halo; R4-R7 = H, halo, haloalkyl, alkoxy, (un)substituted heterocyclyl; X = S(O)n, NHCO, CONH, R8N, R9CH; R8 = H, alkyl; R9 = H, OH; n = 0-2] and their pharmaceutically acceptable salts were prepared NaBH4 was added to 4′-acetyl-2′-[(2,4-difluorophenyl)thio]methanesulfonanilide in MeOH, and the mixture stirred overnight at room temperature and treated with AcOH to give 2′-[(2,4-difluorophenyl)thio]-4′-(1-hydroxyethyl)methanesulfonanilide (II). In rats 10 mg II/kg orally gave 90.1% inhibition of secondary lesions induced by Mycobacterium聽tuberculosis, a measure of antiinflammatory activity. 4′-Acetyl-2′-[(2,4-difluorophenyl)amino]methanesulfonanilide, also prepared, had an analgsic ED50 of 1.8 mg/kg orally in the mouse writhing test. The experimental process involved the reaction of 3-Chloro-4-nitrobenzonitrile(cas: 34662-29-8).Application In Synthesis of 3-Chloro-4-nitrobenzonitrile

The Article related to alkanesulfonanilide preparation analgesic antiinflammatory, Benzene, Its Derivatives, and Condensed Benzenoid Compounds: Sulfenic, Sulfinic, and Sulfonic Acids and Derivatives and other aspects.Application In Synthesis of 3-Chloro-4-nitrobenzonitrile

Referemce:
Nitrile – Wikipedia,
Nitriles – Chemistry LibreTexts

Pippal, Parveen; Singh, Prabal Pratap published an article in 2017, the title of the article was Calcium ferrite, an efficient catalyst for Knoevenagel condensation (A green approach).Quality Control of 2-((1H-Indol-3-yl)methylene)malononitrile And the article contains the following content:

Calcium ferrite NPs catalyst were used as a cheaper and highly efficient catalyst for Knoevenagel condensation of active methylene substrates with various carbonyl compounds affording condensed products in excellent yields in shorter reaction time. The developed greener protocol was very simple, involving cleaner work up and the synthesized products did not require further purification The catalyst was easily removed and reused at least for four times without any appreciable change in reactivity. The experimental process involved the reaction of 2-((1H-Indol-3-yl)methylene)malononitrile(cas: 75629-62-8).Quality Control of 2-((1H-Indol-3-yl)methylene)malononitrile

The Article related to aryl aldehyde active methylene compound calcium ferrite knoevenagel condensation, cyanoalkene preparation green chem, calcium ferrite catalyst preparation crystallinity, Benzene, Its Derivatives, and Condensed Benzenoid Compounds: Hydrocarbons (Saturated and Unsaturated Side Chains) and other aspects.Quality Control of 2-((1H-Indol-3-yl)methylene)malononitrile

Referemce:
Nitrile – Wikipedia,
Nitriles – Chemistry LibreTexts

Badiger, Krishnappa B.; Kamanna, Kantharaju published an article in 2021, the title of the article was Knoevenagel condensation reaction catalysed by agro-waste extract as a greener solvent catalyst.Name: 2-((1H-Indol-3-yl)methylene)malononitrile And the article contains the following content:

This paper present a novel Knoevenagel reaction protocol for the condensation of aromatic/heteroaromatic aldehydes RCHO (R = 2-phenylethenyl, naphthalen-1-yl, furan-2-yl, 1H-indol-3-yl, etc.) with malononitrile to give 伪, 尾-unsaturated benzylidene derivs RCH=C(CN)2. The main focus of this work is to reveal the usability of agro-waste extracts as a catalyst in the Knoevenagel condensation. In addition, the present method describes direct isolation of the formed products without using organic solvent extraction and gives good yields product. The experimental process involved the reaction of 2-((1H-Indol-3-yl)methylene)malononitrile(cas: 75629-62-8).Name: 2-((1H-Indol-3-yl)methylene)malononitrile

The Article related to unsaturated benzylidene preparation green chem, aryl aldehyde malononitrile knoevenagel condensation agro waste extract catalyst, Benzene, Its Derivatives, and Condensed Benzenoid Compounds: Hydrocarbons (Saturated and Unsaturated Side Chains) and other aspects.Name: 2-((1H-Indol-3-yl)methylene)malononitrile

Referemce:
Nitrile – Wikipedia,
Nitriles – Chemistry LibreTexts

On January 31, 2022, Chakraborty, Sourav; Rudra Paul, Abhijit; Majumdar, Swapan published an article.Name: 2-((1H-Indol-3-yl)methylene)malononitrile The title of the article was Base and metal free true recyclable medium for Knoevenagel condensation reaction in SDS-ionic liquid-aqueous miceller composite system. And the article contained the following:

This paper presents for the first time a base and metal free procedure for Knoevenagel condensation reaction in a neutral medium comprises water-SDS-imidazolium ionic liquid composite system. Knoevenagel condensation products from the different aromatic aldehydes and active methylene compounds such as malononitrile, Et cyanoacetate or cyano acetic acid provides good to excellent yields in all cases examined at 80掳C. The developed protocol has several advantages such as chromatog. and organic volatile solvent free protocol, short reaction time and recyclability of catalyst including reaction waste. The reaction is believed to proceed in the hydrophobic cavity of the micelle formed in the medium which was proved by dynamic light scattering studies. The experimental process involved the reaction of 2-((1H-Indol-3-yl)methylene)malononitrile(cas: 75629-62-8).Name: 2-((1H-Indol-3-yl)methylene)malononitrile

The Article related to aryl aldehyde active methylene compound knoevenagel condensation green chem, sds ionic liquid aqueous miceller composite system, Benzene, Its Derivatives, and Condensed Benzenoid Compounds: Hydrocarbons (Saturated and Unsaturated Side Chains) and other aspects.Name: 2-((1H-Indol-3-yl)methylene)malononitrile

Referemce:
Nitrile – Wikipedia,
Nitriles – Chemistry LibreTexts

On December 15, 2010, Chandrappa, S.; Vinaya, K.; Ramakrishnappa, T.; Rangappa, K. S. published an article.Safety of 3-Chloro-4-nitrobenzonitrile The title of the article was An efficient method for aryl nitro reduction and cleavage of azo compounds using iron powder/calcium chloride. And the article contained the following:

A novel, efficient Fe/CaCl2 system was revealed for the reduction of nitro-arenes and reductive cleavage of azo compounds by catalytic transfer hydrogenation. The selective reduction of nitro compounds in the presence of sensitive functional groups including halides, carbonyl, hydroxyl, aldehyde, Me, methoxy, acetyl, nitrile, and ester substituents with an excellent yields is reported. The simple exptl. procedure and easy purification make the protocol advantageous. The experimental process involved the reaction of 3-Chloro-4-nitrobenzonitrile(cas: 34662-29-8).Safety of 3-Chloro-4-nitrobenzonitrile

The Article related to nitro aryl reduction iron calcium chloride catalytic transfer hydrogenation, azo aromatic cleavage iron calcium chloride catalytic transfer hydrogenation, aryl amine preparation and other aspects.Safety of 3-Chloro-4-nitrobenzonitrile

Referemce:
Nitrile – Wikipedia,
Nitriles – Chemistry LibreTexts