2-Bromoacetamide → HCID 66834324, compound

HRID 61723Notes

Reaction equation

HRID 61723 reaction equation
[OH:1][C:2]1[CH:3]=[CH:4][C:5]2[C:17](=[O:18])[C:16]3[C:15]4[C:10](=[CH:11][C:12]([C:19]#[N:20])=[CH:13][CH:14]=4)[NH:9][C:8]=3[C:7]([CH3:22])([CH3:21])[C:6]=2[CH:23]=1.Br[CH2:25][C:26]([NH2:28])=[O:27]>>[C:19]([C:12]1[CH:11]=[C:10]2[C:15]([C:16]3[C:17](=[O:18])[C:5]4[CH:4]=[CH:3][C:2]([O:1][CH2:25][C:26]([NH2:28])=[O:27])=[CH:23][C:6]=4[C:7]([CH3:21])([CH3:22])[C:8]=3[NH:9]2)=[CH:14][CH:13]=1)#[N:20]

Participants

3

Reactant 2

HCID 696322-BromoacetamideHCID 668338618-Hydroxy-6,6-dimethyl-11-oxo-6,11-dihydro-5H-benzo[b]carbazole-3-carbonitrile

Product 1

HCID 66834324HCID 66834324, compound

Procedure

Under the same conditions as the method for synthesizing Compound A7-17, the title compound was prepared from Compound A6 and 2-bromo-acetamide.

Workup

  1. customUnder the same conditions as the method for synthesizing Compound A7-17

Sources & evidence

ORD record
ord-b90b686ed676450b969f86fe07fb4971
Source dataset
uspto-grants-2016_09
Patent number
US09440922B2

Reaction notes

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