5-Aminoisoquinoline → N-(Isoquinolin-5-yl)-2-(decyl)cyclopentane carboxamide
Reaction equation
[CH2:1]([CH:11]1[CH2:15][CH2:14][CH2:13][CH:12]1[C:16]([OH:18])=O)[CH2:2][CH2:3][CH2:4][CH2:5][CH2:6][CH2:7][CH2:8][CH2:9][CH3:10].[NH2:19][C:20]1[CH:29]=[CH:28][CH:27]=[C:26]2[C:21]=1[CH:22]=[CH:23][N:24]=[CH:25]2>>[CH:25]1[C:26]2[C:21](=[C:20]([NH:19][C:16]([CH:12]3[CH2:13][CH2:14][CH2:15][CH:11]3[CH2:1][CH2:2][CH2:3][CH2:4][CH2:5][CH2:6][CH2:7][CH2:8][CH2:9][CH3:10])=[O:18])[CH:29]=[CH:28][CH:27]=2)[CH:22]=[CH:23][N:24]=1Participants
3
Procedure
2-(Decyl)cyclopentane carboxylic acid, prepared according to the procedure of Hoefle, et. al. (U.S. Pat. No. 4,715,175), was coupled with 5-aminoisoquinoline according to the procedure outlined in Example 47 to give the title compound.
Sources & evidence
- ORD record
- ord-e81873c687bd4adab9c410c2f89ee9f5
- Source dataset
- uspto-grants-1994_11
- Patent number
- US05362878
Reaction notes
Loading…