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【结 构 式】

【分子编号】54978

【品名】2-(4-fluoroanilino)-5,6-dimethyl-4-pyrimidinol

【CA登记号】

【 分 子 式 】C12H12FN3O

【 分 子 量 】233.2453032

【元素组成】C 61.79% H 5.19% F 8.15% N 18.02% O 6.86%

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:(XIV)

In an alternative procedure, 4-fluoroaniline (XI) was condensed with cyanamide under acidic conditions to afford the fluorophenyl guanidine (XII). Cyclization of guanidine (XII) with ethyl 2-methylacetoacetate (XIII) in hot DMF produced pyrimidine (XIV). After chlorination of (XIV) with POCl3, the resultant chloropyrimidine (XV) was condensed with tetrahydroisoquinoline (IV) in the presence of either KOAc or Et3N to furnish the title diaminopyrimidine.

1 Lee, Y.N.; Hong, Y.W.; Kim, H.B. (Yuhan Corp.); Process for preparation of pyrmidine derivs.. US 5990311; WO 9742186 .
中间体序号 中间体编号 品名 CAS号 分子式 供应商 用于合成
(IV) 54971 1-methyl-1,2,3,4-tetrahydroisoquinoline C10H13N 详情 详情
(XI) 37690 4-fluorophenylamine; 4-fluoroaniline 371-40-4 C6H6FN 详情 详情
(XII) 54977 N-(4-fluorophenyl)guanidine C7H8FN3 详情 详情
(XIII) 10362 ethyl 2-methyl-3-oxobutanoate; ethyl 2-methylacetoacetate 609-14-3 C7H12O3 详情 详情
(XIV) 54978 2-(4-fluoroanilino)-5,6-dimethyl-4-pyrimidinol C12H12FN3O 详情 详情
(XV) 54979 N-(4-chloro-5,6-dimethyl-2-pyrimidinyl)-N-(4-fluorophenyl)amine; 4-chloro-N-(4-fluorophenyl)-5,6-dimethyl-2-pyrimidinamine C12H11ClFN3 详情 详情
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