反应 #637124

ord-a563abe7bb5a4a0b8d3469d4adec5015

反应方程式

CC(C)(C)OC(=O)N1CCC(c2nc(C=O)cs2)CC1
tert-Butyl 4-(4-formyl-1,3-thiazol-2-yl)piperidine-1-carboxylate
CC(CC[P+](c1ccccc1)(c1ccccc1)c1ccccc1)c1ccccc1.[I-]
triphenyl(3-phenylbutyl)phosphonium iodide
CC(C/C=C\c1csc(C2CCN(C(=O)OC(C)(C)C)CC2)n1)c1ccccc1
tert-Butyl 4-{4-[(1Z)-4-phenylpent-1-en-1-yl]-1,3-thiazol-2-yl}piperidine-1-carboxylate

反应条件

详细条件
See reaction.notes.procedure_details.

后处理

  1. 1
    其他purified

实验过程

tert-Butyl 4-(4-formyl-1,3-thiazol-2-yl)piperidine-1-carboxylate (1.00 g) is reacted with triphenyl(3-phenylbutyl)phosphonium iodide (3.53 g) and purified as described in IV-3. This gives tert-butyl 4-{4-[(1Z)-4-phenylpent-1-en-1-yl]-1,3-thiazol-2-yl}piperidine-1-carboxylate (1.23 g) in form of the Z isomer.

来源

DOI: 10.6084/m9.figshare.5104873.v1专利: US07943774B2uspto-grants-2011_05