Methylamine hydrochloride → HCID 23003369, compound
Reaction equation
[Cl:1][C:2]1[CH:10]=[C:9]2[C:5]([C:6]([CH2:20][C:21]([OH:23])=O)=[C:7]([C:11]([C:13]3[CH:18]=[C:17]([CH3:19])[CH:16]=[CH:15][N:14]=3)=[O:12])[NH:8]2)=[CH:4][CH:3]=1.Cl.[CH3:25][NH2:26]>>[Cl:1][C:2]1[CH:10]=[C:9]2[C:5]([C:6]([CH2:20][C:21]([NH:26][CH3:25])=[O:23])=[C:7]([C:11]([C:13]3[CH:18]=[C:17]([CH3:19])[CH:16]=[CH:15][N:14]=3)=[O:12])[NH:8]2)=[CH:4][CH:3]=1Participants
3
Procedure
The title compound was prepared according to the procedure described in Example 43 from [6-chloro-2-(4-methylpyridine-2-carbonyl)-1H-indol-3-yl]acetic acid (Example 31) and methylamine hydrochloride.
Sources & evidence
- ORD record
- ord-9afd2c06be944683907a1403ff24dd0c
- Source dataset
- uspto-grants-2003_08
- Patent number
- US06608070B1
Reaction notes
Loading…