Trifluoroacetic acid → HCID 178511514, compound
Reaction equation
C(OC(=O)[NH:7][C@H:8]1[CH2:13][CH2:12][C@H:11]([CH2:14][CH2:15][N:16]2[CH2:21][CH2:20][CH:19]([C:22](=[O:31])[C:23]3[CH:28]=[CH:27][C:26]([Cl:29])=[CH:25][C:24]=3[Cl:30])[CH2:18][CH2:17]2)[CH2:10][CH2:9]1)(C)(C)C.FC(F)(F)C(O)=O>>[NH2:7][C@H:8]1[CH2:13][CH2:12][C@H:11]([CH2:14][CH2:15][N:16]2[CH2:17][CH2:18][CH:19]([C:22]([C:23]3[CH:28]=[CH:27][C:26]([Cl:29])=[CH:25][C:24]=3[Cl:30])=[O:31])[CH2:20][CH2:21]2)[CH2:10][CH2:9]1Participants
3
Procedure
The title compound was prepared as described on example 1 from Trans (4-{2-[4-(2,4-Dichloro-benzoyl)-piperidin-1-yl]-ethyl}-cyclohexyl)-carbamic acid tert-butyl ester and trifluoroacetic acid (m/e): 383.3 (M+H+).
Sources & evidence
- ORD record
- ord-5b39acb929164920b1cc7b2b1c3fc0f3
- Source dataset
- uspto-grants-2013_04
- Patent number
- US08415350B2
Reaction notes
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