Chloroform → 3-Chlorobenzenesulphonyl chloride

反応式

[Cl:1]C1C=CC(C)=C(N2CCN([C:14]([C@@H]3[C@H](C4C=CC=C(C)C=4F)CCN([S:30](C(C)C)(=[O:32])=[O:31])C3)=[O:15])CC2)C=1.[Cl:37][C:38]1[CH:39]=[CH:40][C:41](C)=[C:42](N2CCN(C=O)CC2)[CH:43]=1.C(Cl)(Cl)[Cl:54]>>[ClH:1].[CH2:14]=[O:15].[Cl:37][C:38]1[CH:43]=[C:42]([S:30]([Cl:54])(=[O:32])=[O:31])[CH:41]=[CH:40][CH:39]=1

参加物

反応物 3

HCID 6212Chloroform

HCID 68960740HCID 68960740、化合物

HCID 86627852[4-(5-Chloro-2-methyl-phenyl)-piperazin-1-yl]-methanone

生成物 2

HCID 179093-Chlorobenzenesulphonyl chloride

HCID 19933572Methanone hydrochloride

実験手順

In analogy to example 63, step 4, from 4-(5-chloro-2-methyl-phenyl)-piperazin-1-yl]-[(3S,4S) or (3R,4R)-4-(2,4-difluoro-phenyl)-piperidin-3-yl]-methanone hydrochloride and 3-chlorobenzenesulfonyl chloride was prepared [(3S,4S) or (3R,4R)-1-(3-chloro-benzenesulfonyl)-4-(2,4-difluoro-phenyl)-piperidin-3-yl]-[4-(5-chloro-2-methyl-phenyl)-piperazin-1-yl]-methanone as a white foam, MS: 608.0 ([M+H, 1Cl])+; [α]D=+10.71 (c=0.392 g/100 mL, CHCl3).