Bromoacetyl bromide → HCID 10281747, compound
Reaction equation
Br[CH2:2][C:3](Br)=[O:4].[NH2:6][CH:7]1[C:15]2[C:10](=[CH:11][CH:12]=[CH:13][CH:14]=2)[CH2:9][CH2:8]1.[CH3:16][O:17][C:18]1[CH:19]=[C:20]([CH:39]=[CH:40][C:41]=1[O:42][CH3:43])[CH2:21][CH:22]1[C:28]2[CH:29]=[C:30]([O:35][CH3:36])[C:31]([O:33][CH3:34])=[CH:32][C:27]=2[S:26](=[O:38])(=[O:37])[CH2:25][CH2:24][NH:23]1>>[CH3:16][O:17][C:18]1[CH:19]=[C:20]([CH:39]=[CH:40][C:41]=1[O:42][CH3:43])[CH2:21][CH:22]1[C:28]2[CH:29]=[C:30]([O:35][CH3:36])[C:31]([O:33][CH3:34])=[CH:32][C:27]=2[S:26](=[O:38])(=[O:37])[CH2:25][CH2:24][N:23]1[CH2:2][C:3]([NH:6][CH:7]1[C:15]2[C:10](=[CH:11][CH:12]=[CH:13][CH:14]=2)[CH2:9][CH2:8]1)=[O:4]Participants
4
Procedure
prepared by reaction of 2-bromoacetyl bromide with rac-1-aminoindane and 9-(3,4-dimethoxy-benzyl)-2,3-dimethoxy-6,7,8,9-tetrahydro-5-thia-8-aza-benzocycloheptene-5,5-dioxide
Sources & evidence
- ORD record
- ord-255d0961ed6a4cf8b0bbbc3c93f44b74
- Source dataset
- uspto-grants-2007_03
- Patent number
- US07192950B2
Reaction notes
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