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【结 构 式】

【分子编号】62104

【品名】3-ethyl-1-methyl-4-nitro-1H-pyrazole-5-carboxamide

【CA登记号】

【 分 子 式 】C7H10N4O3

【 分 子 量 】198.18156

【元素组成】C 42.42% H 5.09% N 28.27% O 24.22%

与该中间体有关的原料药合成路线共 1 条

合成路线1

该中间体在本合成路线中的序号:(XVIII)

Claisen condensation between diethyl oxalate (X) and 2-butanone (XI) leads to the diketo ester (XII), which is subsequently cyclized with hydrazine hydrate to furnish the pyrazolecarboxylate (XIII). After alkaline hydrolysis of ester (XIII), the resultant pyrazolecarboxylic acid (XIV) is nitrated by fuming HNO3 in hot H2SO4 to provide (XV). Chlorination of acid (XV) with SOCl2, followed by treatment with ammonia in THF yields the pyrazolecarboxamide (XVI). The alkylation of pyrazole (XVI) with iodomethane and Cs2CO3 leads to a mixture of N-methylated regioisomers (XVII) and (XVIII), which are separated by crystallization, followed by column chromatography. The desired isomer (XVII) is further reduced by catalytic hydrogenation to the aminopyrazole (XIX)

1 Street, S.D.A.; Wood, A.; Bunnage, M.E.; Mathias, J.P. (Pfizer Inc.; Pfizer Ltd.); Pyrazolopyrimidinone cGMP PDE5 inhibitors for the treatment of sexual dysfunction. WO 9954333 .
中间体序号 中间体编号 品名 CAS号 分子式 供应商 用于合成
(X) 17571 Diethyl oxalate; Ethyl 2-ethoxy-2-oxoacetate 95-92-1 C6H10O4 详情 详情
(XI) 33891 Methyl ethyl ketone; 2-Butanone 78-93-3 C4H8O 详情 详情
(XII) 62099 ethyl 2,4-dioxohexanoate C8H12O4 详情 详情
(XIII) 62100 ethyl 3-ethyl-1H-pyrazole-5-carboxylate C8H12N2O2 详情 详情
(XIV) 62101 3-ethyl-1H-pyrazole-5-carboxylic acid C6H8N2O2 详情 详情
(XV) 62102 3-ethyl-4-nitro-1H-pyrazole-5-carboxylic acid C6H7N3O4 详情 详情
(XVI) 62103 3-ethyl-4-nitro-1H-pyrazole-5-carboxamide C6H8N4O3 详情 详情
(XVII) 62105 5-ethyl-1-methyl-4-nitro-1H-pyrazole-3-carboxamide C7H10N4O3 详情 详情
(XVIII) 62104 3-ethyl-1-methyl-4-nitro-1H-pyrazole-5-carboxamide C7H10N4O3 详情 详情
(XIX) 62106 4-amino-5-ethyl-1-methyl-1H-pyrazole-3-carboxamide C7H12N4O 详情 详情
Extended Information