4-(Trifluoromethoxy)aniline → HCID 49804514, 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]=[C:21]([C:23]([F:26])([F:25])[F:24])[CH:20]=[CH:19][C:18]=1[S:27](Cl)(=[O:29])=[O:28].[F:31][C:32]([F:42])([F:41])[O:33][C:34]1[CH:40]=[CH:39][C:37]([NH2:38])=[CH:36][CH:35]=1>>[Cl:16][C:17]1[CH:22]=[C:21]([C:23]([F:26])([F:25])[F:24])[CH:20]=[CH:19][C:18]=1[S:27]([N:9]1[CH2:8][CH2:7][C:6]2([C:4](=[O:5])[N:38]([C:37]3[CH:39]=[CH:40][C:34]([O:33][C:32]([F:31])([F:41])[F:42])=[CH:35][CH:36]=3)[CH2:13][CH2:12]2)[CH2:11][CH2:10]1)(=[O:29])=[O:28]Participants
4
Procedure
White solid. MS (ESI): 557.07 (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-chloro-4-trifluoromethyl-benzenesulfonyl chloride and 4-(trifluoromethoxy)-aniline.
Sources & evidence
- ORD record
- ord-4ced7e2929014371baaabfad87050531
- Source dataset
- uspto-grants-2012_12
- Patent number
- US08329904B2
Reaction notes
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