Propylamine → HCID 77750506, compound
Reaction equation
[OH:1][CH:2]1[CH:6]([OH:7])[CH:5]([N:8]2[C:12]3[N:13]=[C:14]([S:27][CH3:28])[N:15]=[C:16]([NH:17][CH:18]4[CH2:20][CH:19]4[C:21]4[CH:26]=[CH:25][CH:24]=[CH:23][CH:22]=4)[C:11]=3[N:10]=[N:9]2)[CH2:4][CH:3]1[C:29]([NH:31][C:32]1C=CC=[CH:34][CH:33]=1)=[O:30].C(N)CC>>[OH:1][CH:2]1[CH:6]([OH:7])[CH:5]([N:8]2[C:12]3[N:13]=[C:14]([S:27][CH3:28])[N:15]=[C:16]([NH:17][CH:18]4[CH2:20][CH:19]4[C:21]4[CH:22]=[CH:23][CH:24]=[CH:25][CH:26]=4)[C:11]=3[N:10]=[N:9]2)[CH2:4][CH:3]1[C:29]([NH:31][CH2:32][CH2:33][CH3:34])=[O:30]Participants
3
Procedure
The subtitle compound was prepared according to the method of example 39, step a) using the product of example 20, step b) and propylamine.
Sources & evidence
- ORD record
- ord-e70841f5ad2c44599c5ca7b1d68d7a3b
- Source dataset
- uspto-grants-2002_04
- Patent number
- US06369064B1
Reaction notes
Loading…