2-Trifluoromethylbenzenesulphonyl chloride → 2-(4-Isopropoxy-phenyl)-8-(2-trifluoromethyl-benzenesulfonyl)-2,8-diaza-spiro[4.5]decan-1-one

HRID 2194087Notes

Reaction equation

HRID 2194087 reaction equation
C(O[C:4]([C:6]1([CH2:12][CH2:13]OC)[CH2:11][CH2:10][NH:9][CH2:8][CH2:7]1)=[O:5])C.[F:16][C:17]([F:29])([F:28])[C:18]1[CH:23]=[CH:22][CH:21]=[CH:20][C:19]=1[S:24](Cl)(=[O:26])=[O:25].F[C:31](F)(F)[CH:32]([CH3:41])[O:33][C:34]1[CH:39]=[CH:38][C:37]([NH2:40])=[CH:36][CH:35]=1>>[CH:32]([O:33][C:34]1[CH:39]=[CH:38][C:37]([N:40]2[CH2:13][CH2:12][C:6]3([CH2:7][CH2:8][N:9]([S:24]([C:19]4[CH:20]=[CH:21][CH:22]=[CH:23][C:18]=4[C:17]([F:29])([F:28])[F:16])(=[O:26])=[O:25])[CH2:10][CH2:11]3)[C:4]2=[O:5])=[CH:36][CH:35]=1)([CH3:41])[CH3:31]

Participants

4

Procedure

Light brown solid. MS (ESI): 551.14 (MH+). This example was prepared in analogy to example 1 step C) to D) from 4-(2-methoxy-ethyl)-piperidine-4-carboxylic acid ethyl ester (example 1 step B)), 2-trifluoromethyl-benzenesulfonyl chloride, 4-(2,2,2-trifluoro-1-methyl-ethoxy)-phenylamine.

Sources & evidence

ORD record
ord-2d453c8579dc4c219bd81fcd04a925e3
Source dataset
uspto-grants-2012_12
Patent number
US08329904B2

Reaction notes

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