N-bromobutanimide → HCID 21498890, compound

HRID 1730052Notes

Reaction equation

[N+:1]([C:4]1[CH:5]=[CH:6][C:7]([N:18]2[CH:22]=[N:21][N:20]=[C:19]2[CH2:23][N:24]2[C:28](=[O:29])[C:27]3=[CH:30][CH:31]=[CH:32][CH:33]=[C:26]3[C:25]2=[O:34])=[C:8]([CH:17]=1)[C:9]([C:11]1[CH:16]=[CH:15][CH:14]=[CH:13][CH:12]=1)=[O:10])([O-:3])=[O:2].[Br:35]N1C(=O)CCC1=O>>[N+:1]([C:4]1[CH:5]=[CH:6][C:7]([N:18]2[C:19]([CH2:23][N:24]3[C:25](=[O:34])[C:26]4=[CH:33][CH:32]=[CH:31][CH:30]=[C:27]4[C:28]3=[O:29])=[N:20][N:21]=[C:22]2[Br:35])=[C:8]([CH:17]=1)[C:9]([C:11]1[CH:12]=[CH:13][CH:14]=[CH:15][CH:16]=1)=[O:10])([O-:3])=[O:2]

Participants

Reactant 2

HCID 67184N-bromobutanimide

HCID 21498875HCID 21498875, compound

Product 1

HCID 21498890HCID 21498890, compound

Procedure

Following the procedure of Example 2, 5-nitro-2-[3-phthalimidomethyl-4H-1,2,4-triazol-4-yl]benzophenone is reacted with N-bromosuccinimide to form 5-nitro-2-[3-bromo-5-phthalimidomethyl-4H-1,2,4-triazol-4-yl]benzophenone.

Sources & evidence

ORD record: ord-da99855c19524c1981666ef4c7de9f00
Source dataset: uspto-grants-1976_11
DOI: 10.6084/m9.figshare.5104873.v1
Patent number: US03991070

Reaction notes

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