2-Chlorobenzenesulfonyl chloride → HCID 59577943, compound
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.[Cl:16][C:17]1[CH:22]=[CH:21][CH:20]=[CH:19][C:18]=1[S:23](Cl)(=[O:25])=[O:24].[CH:27]1([CH2:32][O:33][C:34]2[CH:39]=[CH:38][C:37]([NH2:40])=[CH:36][CH:35]=2)[CH2:31][CH2:30][CH2:29][CH2:28]1>>[Cl:16][C:17]1[CH:22]=[CH:21][CH:20]=[CH:19][C:18]=1[S:23]([N:9]1[CH2:8][CH2:7][C:6]2([C:4](=[O:5])[N:40]([C:37]3[CH:36]=[CH:35][C:34]([O:33][CH2:32][CH:27]4[CH2:28][CH2:29][CH2:30][CH2:31]4)=[CH:39][CH:38]=3)[CH2:13][CH2:12]2)[CH2:11][CH2:10]1)(=[O:25])=[O:24]Participants
4
Procedure
Light Brown crystalline solid. MS (ESI): 503.2 (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-chlorobenzenesulfonyl chloride and 4-cyclopentylmethoxy-phenylamine.
Sources & evidence
- ORD record
- ord-6e0ef324c5944021b977956e3332a69f
- Source dataset
- uspto-grants-2012_12
- Patent number
- US08329904B2
Reaction notes
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