4-Chlorobenzoyl chloride → HCID 178519591, compound
Reaction equation
[CH:1]1([NH:7][C@H:8]2[CH2:13][CH2:12][C@H:11]([C:14]3[CH:19]=[CH:18][CH:17]=[CH:16][CH:15]=3)[CH2:10][CH2:9]2)[CH2:6][CH2:5][CH2:4][CH2:3][CH2:2]1.[Cl:20][C:21]1[CH:29]=[CH:28][C:24]([C:25](Cl)=[O:26])=[CH:23][CH:22]=1>>[Cl:20][C:21]1[CH:29]=[CH:28][C:24]([C:25]([N:7]([C@H:8]2[CH2:9][CH2:10][C@H:11]([C:14]3[CH:15]=[CH:16][CH:17]=[CH:18][CH:19]=3)[CH2:12][CH2:13]2)[CH:1]2[CH2:2][CH2:3][CH2:4][CH2:5][CH2:6]2)=[O:26])=[CH:23][CH:22]=1Participants
3
Procedure
from trans-N-cyclohexyl-4-phenylcyclohexylamine and 4-chlorobenzoylchloride. Melting point: 164°-166° C.
Sources & evidence
- ORD record
- ord-06a8c2d6b9814896ba0e21e7dcbcfe1b
- Source dataset
- uspto-grants-1995_10
- Patent number
- US05455273
Reaction notes
Loading…