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【结 构 式】

【分子编号】51144

【品名】ethyl 4,6-dihydroxy-2-(4-methoxybenzyl)-2H-pyrazolo[3,4-b]pyridine-5-carboxylate

【CA登记号】

【 分 子 式 】C17H17N3O5

【 分 子 量 】343.3392

【元素组成】C 59.47% H 4.99% N 12.24% O 23.3%

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:(VI)

3-Amino-4-carbethoxypyrazole (I) was protected with p-methoxybenzyl chloride (II) in the presence of NaH to give two alkylated regioisomers (III) and (IV). This mixture was subjected to condensation with diethyl malonate under basic conditions to furnish the respective pyrazolopyridines (V) and (VI). Only isomer (VI) could be converted to its corresponding dichloro derivative (VII) under reflux in POCl3. Regioselective displacement of one chloride group from (VII) with ethanolic ammonia afforded amine (VIII). The ester group of (VIII) was then hydrolyzed by LiOH to the carboxylic acid (IX), which was converted to amide (X) via activation as the pentafluorophenyl ester.

1 Bi, Y.; et al.; The discovery of novel, potent and selective PDE5 inhibitors. Bioorg Med Chem Lett 2001, 11, 18, 2461.
中间体序号 中间体编号 品名 CAS号 分子式 供应商 用于合成
(I) 51140 3-Amino-4-pyrazolecarboxylic acid ethyl ester; Ethyl 3-aminopyrazole-4-carboxylate; 3-Amino-4-carbethoxypyrazole 6994-25-8 C6H9N3O2 详情 详情
(II) 11910 4-Methoxybenzyl chloride; 1-(Chloromethyl)-4-methoxybenzene; alpha-Chloro-4-methoxytoluene; 4-(Chloromethyl)phenyl methyl ether 824-94-2 C8H9ClO 详情 详情
(III) 51141 ethyl 5-amino-1-(4-methoxybenzyl)-1H-pyrazole-4-carboxylate C14H17N3O3 详情 详情
(IV) 51142 ethyl 3-amino-1-(4-methoxybenzyl)-1H-pyrazole-4-carboxylate C14H17N3O3 详情 详情
(V) 51143 ethyl 4,6-dihydroxy-1-(4-methoxybenzyl)-1H-pyrazolo[3,4-b]pyridine-5-carboxylate C17H17N3O5 详情 详情
(VI) 51144 ethyl 4,6-dihydroxy-2-(4-methoxybenzyl)-2H-pyrazolo[3,4-b]pyridine-5-carboxylate C17H17N3O5 详情 详情
(VII) 51145 ethyl 4,6-dichloro-2-(4-methoxybenzyl)-2H-pyrazolo[3,4-b]pyridine-5-carboxylate C17H15Cl2N3O3 详情 详情
(VIII) 51146 ethyl 4-amino-6-chloro-2-(4-methoxybenzyl)-2H-pyrazolo[3,4-b]pyridine-5-carboxylate C17H17ClN4O3 详情 详情
(IX) 51147 4-amino-6-chloro-2-(4-methoxybenzyl)-2H-pyrazolo[3,4-b]pyridine-5-carboxylic acid C15H13ClN4O3 详情 详情
(X) 51148 4-amino-6-chloro-2-(4-methoxybenzyl)-2H-pyrazolo[3,4-b]pyridine-5-carboxamide C15H14ClN5O2 详情 详情
Extended Information