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【结 构 式】

【分子编号】29010

【品名】6-(2-hydroxyethyl)-7-methyl-2,3-dihydro-5H-[1,3]thiazolo[3,2-a]pyrimidin-5-one

【CA登记号】

【 分 子 式 】C9H12N2O2S

【 分 子 量 】212.27256

【元素组成】C 50.92% H 5.7% N 13.2% O 15.07% S 15.11%

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:(III)

By condensation of 4-(4-fluorobenzoyl)piperidine (IX) with 6-(2-bromo ethyl)-7-methyl-2,3-dihydro-5H-thiazolo[2,3-a]pyrimidin-5-one (IV) by means of Na2CO3 in refluxing 4-methyl-2-pentanone. The starting products are obtained as follows: The cyclization of 4-hydroxy-5-(2-hydroxyethyl)-6-methyl-2-mercaptopyrimidine (I) with 1,2-dibromo ethane (II) by means of K2CO3 in hot dimethylacetamide gives 2,3-dihydro-6-(2-hydroxyethyl)-7-methyl-5H-thiazolo[3,2-a]pyrimidin-5-one (II), which by reaction with HBr in refluxing acetic acid is converted to the corresponding 6-(2-bromoethyl) derivative (IV). The Grignard reaction of 4-bromofluorobenzene (V) with N benzyl-4 cyanopiperidine (VI) by means of Mg in dimethoxyethane gives 4-(4-fluorobenzoyl)-N-benzylpiperidine (VII), which is treated with ethyl chlorocarbo-nate in refluxing toluene to afford ethyl 4-(4-fluorobenzoyl)piperidine-1-carboxylate (VIII). Finally, this compound is treated with HBr in refluxing 48% HBr to give (IX).

1 Kennis, L.; Mertens, J.C. (Janssen Pharmaceutica NV); Bicyclic pyrimidin-5-one derivatives. DD 215553; EP 0070053; US 4443451 .
2 Serradell, M.N.; Castaner, J.; Setoperone. Drugs Fut 1985, 10, 1, 40.
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) 29009 5-(2-hydroxyethyl)-6-methyl-2-sulfanyl-4-pyrimidinol C7H10N2O2S 详情 详情
(II) 10252 1,2-Dibromoethane; Ethylene dibromide 106-93-4 C2H4Br2 详情 详情
(III) 29010 6-(2-hydroxyethyl)-7-methyl-2,3-dihydro-5H-[1,3]thiazolo[3,2-a]pyrimidin-5-one C9H12N2O2S 详情 详情
(IV) 29011 6-(2-bromoethyl)-7-methyl-2,3-dihydro-5H-[1,3]thiazolo[3,2-a]pyrimidin-5-one C9H11BrN2OS 详情 详情
(V) 29012 1-bromo-4-fluorobenzene 460-00-4 C6H4BrF 详情 详情
(VI) 29013 1-benzyl-4-piperidinecarbonitrile C13H16N2 详情 详情
(VII) 29014 (1-benzyl-4-piperidinyl)(4-fluorophenyl)methanone C19H20FNO 详情 详情
(VIII) 29015 ethyl 4-(4-fluorobenzoyl)-1-piperidinecarboxylate C15H18FNO3 详情 详情
(IX) 21497 (4-Fluorophenyl)(4-piperidinyl)methanone; 4-(4-Fluorobenzoyl)piperidine; 4-(p-Fluorobenzoyl)piperidine 56346-57-7 C12H14FNO 详情 详情
Extended Information