Bromoacetyl bromide → HCID 10119840, compound

HRID 458820Notes

Reaction equation

HRID 458820 reaction equation
Br[CH2:2][C:3](Br)=[O:4].[CH3:6][C:7]1[CH:15]=[CH:14][CH:13]=[C:12]2[C:8]=1[CH2:9][CH2:10][CH:11]2[NH2:16].[CH3:17][O:18][C:19]1[CH:20]=[C:21]([CH:38]=[CH:39][C:40]=1[O:41][CH3:42])[CH2:22][CH:23]1[C:29]2[CH:30]=[C:31]([O:36][CH3:37])[C:32]([O:34][CH3:35])=[CH:33][C:28]=2[CH2:27][CH2:26][CH2:25][NH:24]1>>[CH3:17][O:18][C:19]1[CH:20]=[C:21]([CH:38]=[CH:39][C:40]=1[O:41][CH3:42])[CH2:22][CH:23]1[C:29]2[CH:30]=[C:31]([O:36][CH3:37])[C:32]([O:34][CH3:35])=[CH:33][C:28]=2[CH2:27][CH2:26][CH2:25][N:24]1[CH2:2][C:3]([NH:16][CH:11]1[C:12]2[C:8](=[C:7]([CH3:6])[CH:15]=[CH:14][CH:13]=2)[CH2:9][CH2:10]1)=[O:4]

Participants

4

Procedure

prepared by reaction of 2-bromoacetyl bromide with rac-4-methyl-indan-1-ylamine and 1-(3,4-dimethoxy-benzyl)-7,8-dimethoxy-2,3,4,5-tetrahydro-1H-benzo[c]azepine.

Sources & evidence

ORD record
ord-62a92916ce2f47a4af0e5a601ad09b64
Source dataset
uspto-grants-2007_03
Patent number
US07192950B2

Reaction notes

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