1083158-66-0

Basic information

• Product Name: N-[2-methyl-4-(1-methylbenzimidazole)-2-yl-6-nitrophenyl]-butanamide
• Synonyms: N-[2-methyl-4-(1-methylbenzimidazole)-2-yl-6-nitrophenyl]-butanamide
• CAS NO: 1083158-66-0
• Molecular Weight: 352.393
• Mol File: 1083158-66-0.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: N-[2-methyl-4-(1-methylbenzimidazole)-2-yl-6-nitrophenyl]-butanamide(CAS DataBase Reference)
• NIST Chemistry Reference: N-[2-methyl-4-(1-methylbenzimidazole)-2-yl-6-nitrophenyl]-butanamide(1083158-66-0)
• EPA Substance Registry System: N-[2-methyl-4-(1-methylbenzimidazole)-2-yl-6-nitrophenyl]-butanamide(1083158-66-0)

Safety Data

• Hazardous Substances Data: 1083158-66-0(Hazardous Substances Data)

Upstream product

• 1016696-74-4 N-butyryl-4-amino-3-methylbenzoic acid 
• 3113-71-1 3-methyl-4-nitrobenzoic acid 
• 2486-70-6 4-amino 3-methylbenzoic acid 
• 959987-48-5 N-butyryl-4-amino-3-methyl-5-nitrobenzoic acid 
• 4760-34-3 N-methyl-1,2-phenylenediamine 
• 959987-49-6 N-(2-aminophenyI)-4-(butyramido)-N,3-dimethyl-5-nitrobenzamide 

Downstream Products

• 1083158-65-9 1-[4-N-butyrylamino-3-methyl-5-aminophenyl]-3N-methylbenzimidazole 
• 152628-02-9 2-n-propyl-4-methyl-6-(1-methylbenzimidazol-2-yl)benzimidazole 

Relevant articles and documents

Synthetic method 2 - n-propyl -4 - methyl -6 - (1 -methylbenzimidazole -2 -yl) benzimidazole (by machine translation)

The invention relates to the technical field of synthesis of medical intermediates, and discloses a synthesis method of 2 - n-propyl -4 - methyl -6 - (1 -methylbenzimidazole -2 -yl) benzimidazole; S1: a condensation closed loop is obtained; and the reaction temperature is controlled to 3 - and the intermediate IV is N - [-4 - methyl -5 - (40 - 110 °C-methylbenzimidazole) 2 -nitrophenyl]-butylamide; S2: a reduction ring; and the preparation method comprises the following steps: S3: condensation ring-ring synthesis and intermediate IV of -4 -propyl -4 - 1 -6 - methyl 1 - S4 -2 - (-6 -methylbenzimidazol 2 -yl) benzimidazole -2 . 2 - N-propyl -4 - methyl -6 - (1 -methylbenzimidazole -2 -yl) benzimidazole is higher in purity, reduced in impurities and high in yield. (by machine translation)

Concise synthesis of telmisartan via decarboxylative cross-coupling

(Chemical Equation Presented) An efficient synthesis of the angiotensin II receptor antagonist telmisartan is presented involving a decarboxylative cross-coupling of isopropyl phthalate (1) with 2-(4-chlorophenyl)-1,3-dioxolane (2c) as the key step (85% yield). The benzimidazole moiety is constructed regioselectively via a reductive animation-condensation sequence, replacing the previously published route via alkylation of the preformed benzimidazole. The product is obtained in an overall yield of 35% in a convergent synthesis with the longest sequence consisting of eight steps.