2-Bromoacetamide → HCID 135979632, compound

HRID 1784021Notes

Reaction equation

HRID 1784021 reaction equation
C([N:4]1[CH2:9][CH2:8][CH:7]([C:10]2[CH:15]=[CH:14][C:13]([NH:16][C:17]3[C:18]4[N:19]([N:28]=[CH:29][N:30]=4)[C:20]([C:23]4[CH:24]=[N:25][NH:26][CH:27]=4)=[CH:21][N:22]=3)=[CH:12][CH:11]=2)[CH2:6][CH2:5]1)(C)C.Br[CH2:32][C:33]([NH2:35])=[O:34]>>[NH:26]1[CH:27]=[C:23]([C:20]2[N:19]3[N:28]=[CH:29][N:30]=[C:18]3[C:17]([NH:16][C:13]3[CH:12]=[CH:11][C:10]([CH:7]4[CH2:8][CH2:9][N:4]([CH2:32][C:33]([NH2:35])=[O:34])[CH2:5][CH2:6]4)=[CH:15][CH:14]=3)=[N:22][CH:21]=2)[CH:24]=[N:25]1

Participants

3

Procedure

This compound may be prepared using methods as described for Compound 84, using 2-bromoacetamide in step 1. LCMS: Rt=0.81 min (100%), m/z (ESI) 418 (M+H)+.

Workup

  1. customThis compound may be prepared

Sources & evidence

ORD record
ord-412c6895c66746fb9d5be9457be48763
Source dataset
uspto-grants-2009_03
Patent number
US07501411B2

Reaction notes

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