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【结 构 式】

【分子编号】24705

【品名】1-benzyl-4-[bis(4-fluorophenyl)methylene]piperidine

【CA登记号】

【 分 子 式 】C25H23F2N

【 分 子 量 】375.4611664

【元素组成】C 79.97% H 6.17% F 10.12% N 3.73%

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:(IV)

The Grignard condensation of ethyl 1-benzyl-piperidine-4-carboxylate (I) with 4-fluorophenylmagnesium bromide (II) in THF gives a-bis(4-fluorophenyl)-1-benzylpiperidine-4-methanol (III), which is dehydrated with HCl in refluxing acetic acid yielding 1-benzyl-4-[bis(4 fluorophenyl)methylene]piperidine (IV). Elimination of the benzyl group of (IV) by hydrogenation with H2 over rhodium/carbon in methanol affords 4-[bis(4 fluorophenyl)metlylene] piperidine (V), which is finally condensed with 6-(2-chloroethyl)-7-methyl 5H thiazolo[3,2-a]pyrimidin-5-one (VI) by means of Na2CO3 and KI lo refluxing 4-methyl-2-pentanone. Compound (VI) is obtained by cyclocondensation of 2-thiazolylamine (VII) with 3 acetyl 4,5 dihydro-2(3H)furanone (VIII) by means of aqueous concentrated HCl in refluxing toluene.

1 Kennis, L.E.J.; Mertens, J.C.; Vandenberk, J. (Janssen Pharmaceutica NV); Novel ((bis(aryl)methylene)-1-piperidinyl)alkyl-pyrimidinones. EP 0110435; ES 8601965; US 4485107 .
2 Prous, J.; Castaner, J.; Ritanserin. Drugs Fut 1986, 11, 5, 391.
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) 22600 ethyl 1-benzyl-4-piperidinecarboxylate; N-Benzyl-4-carbethoxy piperidine 24228-40-8 C15H21NO2 详情 详情
(II) 13643 4-fluorophenyl magnesium bromide;Bromo(4-fluorophenyl)magnesium;bromo(p-fluorophenyl)Magnesium;p-Fluorophenylmagnesium bromide 352-13-6 C6H4BrFMg 详情 详情
(III) 22601 (1-benzyl-4-piperidinyl)[bis(4-fluorophenyl)]methanol C25H25F2NO 详情 详情
(IV) 24705 1-benzyl-4-[bis(4-fluorophenyl)methylene]piperidine C25H23F2N 详情 详情
(V) 24706 4-[bis(4-fluorophenyl)methylene]piperidine C18H17F2N 详情 详情
(VI) 24707 6-(2-chloroethyl)-7-methyl-5H-[1,3]thiazolo[3,2-a]pyrimidin-5-one C9H9ClN2OS 详情 详情
(VIII) 24709 3-acetyldihydro-2(3H)-furanone 517-23-7 C6H8O3 详情 详情
Extended Information