Cyclohexylamine → 1-Chloro-N-cyclohexyl-5-methylisoquinolin-4-carboxamide
Reaction equation
[Cl:1][C:2]1[C:11]2[C:6](=[C:7]([CH3:12])[CH:8]=[CH:9][CH:10]=2)[C:5]([C:13]([OH:15])=O)=[CH:4][N:3]=1.[CH:16]1([NH2:22])[CH2:21][CH2:20][CH2:19][CH2:18][CH2:17]1>>[Cl:1][C:2]1[C:11]2[C:6](=[C:7]([CH3:12])[CH:8]=[CH:9][CH:10]=2)[C:5]([C:13]([NH:22][CH:16]2[CH2:21][CH2:20][CH2:19][CH2:18][CH2:17]2)=[O:15])=[CH:4][N:3]=1Participants
3
Procedure
This compound was prepared by using 1-chloro-5-methylisoquinolin-4-carboxylic acid (Intermediate-10) and cyclohexylamine by following the similar procedure as described for intermediate-11a.
Workup
- customThis compound was prepared
Sources & evidence
- ORD record
- ord-d0ce764f74ad4bafb2387ca3ccb2446e
- Source dataset
- uspto-grants-2015_04
- Patent number
- US09006442B2
Reaction notes
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