Tert-Butylamine → N-(tert-Butyl)-1-chloro-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.[C:16]([NH2:20])([CH3:19])([CH3:18])[CH3:17]>>[C:16]([NH:20][C:13]([C:5]1[C:6]2[C:11](=[CH:10][CH:9]=[CH:8][C:7]=2[CH3:12])[C:2]([Cl:1])=[N:3][CH:4]=1)=[O:15])([CH3:19])([CH3:18])[CH3:17]Participants
3
Procedure
This compound was prepared by using 1-chloro-5-methylisoquinolin-4-carboxylic acid (Intermediate-10) and tert-butylamine by following the similar procedure as described for Intermediate-11a.
Workup
- customThis compound was prepared
Sources & evidence
- ORD record
- ord-90a383639ddd451ab48973b63ce757a0
- Source dataset
- uspto-grants-2015_04
- Patent number
- US09006442B2
Reaction notes
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