Methyl Bromide → HCID 21489199, compound

HRID 1974278Notes

Reaction equation

[CH2:1]([C:3]1[CH:4]=[C:5]2[C:10](=[CH:11][CH:12]=1)[N:9]=[C:8]1[NH:13][C:14]3[CH:19]=[C:18]([CH3:20])[C:17]([CH3:21])=[CH:16][C:15]=3[N:7]1[C:6]2=[O:22])[CH3:2].[CH3:23]Br>>[CH2:1]([C:3]1[CH:4]=[C:5]2[C:10](=[CH:11][CH:12]=1)[N:9]=[C:8]1[N:13]([CH3:23])[C:14]3[CH:19]=[C:18]([CH3:20])[C:17]([CH3:21])=[CH:16][C:15]=3[N:7]1[C:6]2=[O:22])[CH3:2]

Participants

Reactant 2

HCID 6323Methyl Bromide

HCID 21489180HCID 21489180, compound

Product 1

HCID 21489199HCID 21489199, compound

Procedure

2-Ethyl-6,8,9-Trimethylbenzimidazo[2,1-b]quinazoline-12(6H)one is prepared with 2-ethyl-8,9-dimethylbenzimidazo[2,1-b]-quinazolin-12(6H)one and methyl bromide.

Sources & evidence

ORD record: ord-4ae0b578ac4d47d8a1000b92ed693c23
Source dataset: uspto-grants-1976_12
DOI: 10.6084/m9.figshare.5104873.v1
Patent number: US04000275

Reaction notes

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