4-Chlorobenzoyl chloride → HCID 178457686, compound
Reaction equation
[CH:1]([NH:4][C@H:5]1[CH2:10][CH2:9][C@H:8]([C:11]2[CH:16]=[CH:15][CH:14]=[CH:13][CH:12]=2)[CH2:7][CH2:6]1)([CH3:3])[CH3:2].[Cl:17][C:18]1[CH:26]=[CH:25][C:21]([C:22](Cl)=[O:23])=[CH:20][CH:19]=1>>[Cl:17][C:18]1[CH:26]=[CH:25][C:21]([C:22]([N:4]([C@H:5]2[CH2:6][CH2:7][C@H:8]([C:11]3[CH:16]=[CH:15][CH:14]=[CH:13][CH:12]=3)[CH2:9][CH2:10]2)[CH:1]([CH3:3])[CH3:2])=[O:23])=[CH:20][CH:19]=1Participants
3
Procedure
from trans-N-isopropyl-4-phenylcyclohexylamine and 4-chlorobenzoylchloride. Melting point: 130°-132° C.
Sources & evidence
- ORD record
- ord-fe745804491648c4824347325b9fb0c6
- Source dataset
- uspto-grants-1995_10
- Patent number
- US05455273
Reaction notes
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