2-Amino-N,N-dimethylethane-1-sulfonamide → HCID 67198952, compound
Reaction equation
[CH2:1]([O:3][C:4]1[CH:5]=[C:6]([CH:23]=[CH:24][C:25]=1[O:26][CH2:27][CH3:28])[CH2:7][C:8]1[O:12][N:11]=[C:10]([C:13]2[CH:21]=[CH:20][CH:19]=[C:18]3[C:14]=2[CH2:15][CH2:16][CH:17]3O)[N:9]=1)[CH3:2].[NH2:29][CH2:30][CH2:31][S:32]([N:35](C)[CH3:36])(=[O:34])=[O:33]>>[CH2:1]([O:3][C:4]1[CH:5]=[C:6]([CH:23]=[CH:24][C:25]=1[O:26][CH2:27][CH3:28])[CH2:7][C:8]1[O:12][N:11]=[C:10]([C:13]2[CH:21]=[CH:20][CH:19]=[C:18]3[C:14]=2[CH2:15][CH2:16][CH:17]3[NH:29][CH2:30][CH2:31][S:32]([NH:35][CH3:36])(=[O:34])=[O:33])[N:9]=1)[CH3:2]Participants
3
Procedure
Prepared using General Procedure 14 from 4-(5-(3,4-diethoxybenzyl)-1,2,4-oxadiazol-3-yl)-2,3-dihydro-1H-inden-1-ol 60 and 2-amino-N,N-dimethylethanesulfonamide.
Workup
- customPrepared
Sources & evidence
- ORD record
- ord-e805c42b98784f6db2c1b3a60a2a31c3
- Source dataset
- uspto-grants-2013_01
- Patent number
- US08357706B2
Reaction notes
Loading…