1-methanesulfonyl-3-methyl-6-amino-1H-indole → HCID 178430979, compound
Reaction equation
[CH3:1][S:2]([N:5]1[C:13]2[C:8](=[CH:9][CH:10]=[C:11]([NH2:14])[CH:12]=2)[C:7]([CH3:15])=[CH:6]1)(=[O:4])=[O:3].[ClH:16].CS(N1C2C(=CC=C(N=[C:31]3[NH:35][CH2:34][CH2:33][NH:32]3)C=2)C=C1)(=O)=O>>[ClH:16].[NH:32]1[CH2:33][CH2:34][NH:35][C:31]1=[N:14][C:11]1[CH:12]=[C:13]2[C:8]([C:7]([CH3:15])=[CH:6][N:5]2[S:2]([CH3:1])(=[O:4])=[O:3])=[CH:9][CH:10]=1Participants
3
Procedure
Imidazolidin-2-ylidene-(1-methanesulfonyl-3-methyl-1H-indol-6-yl)-amine hydrochloride (mp 236.4-236.7° C.) was prepared from 1-methanesulfonyl-3-methyl-6-amino-1H-indole by a procedure which was similar to that for the preparation of N-methanesulfonyl-6-(imidazolidin-2-ylideneamino)indole hydrochloride.
Sources & evidence
- ORD record
- ord-b3cba9607cb94173be707c6c93bbbdcb
- Source dataset
- uspto-grants-2000_05