1-Bromo-2-methylpropane → HCID 21489220, compound

HRID 1974281Notes

Reaction equation

HRID 1974281 reaction equation
[CH2:1]([O:3][C:4]1[CH:13]=[C:12]2[C:7]([C:8](=[O:23])[N:9]3[C:16]4[CH:17]=[C:18]([CH3:22])[C:19]([CH3:21])=[CH:20][C:15]=4[NH:14][C:10]3=[N:11]2)=[CH:6][CH:5]=1)[CH3:2].[CH2:24](Br)[CH:25]([CH3:27])[CH3:26]>>[CH2:1]([O:3][C:4]1[CH:13]=[C:12]2[C:7]([C:8](=[O:23])[N:9]3[C:16]4[CH:17]=[C:18]([CH3:22])[C:19]([CH3:21])=[CH:20][C:15]=4[N:14]([CH2:24][CH:25]([CH3:27])[CH3:26])[C:10]3=[N:11]2)=[CH:6][CH:5]=1)[CH3:2]

Participants

3

Reactant 2

HCID 65551-Bromo-2-methylpropaneHCID 21489173HCID 21489173, compound

Product 1

HCID 21489220HCID 21489220, compound

Procedure

3-Ethoxy-6-isobutyl-8,9-dimethylbenzimidazo[2,1-b]-quinazolin-12(6H)one is prepared with 3-ethoxy-8,9-dimethylbenzimidazo[2,1-b]quinazolin-12(6H)one and isobutyl bromide.

Sources & evidence

ORD record
ord-078c1cab2c034b0cacf7755e392f6e43
Source dataset
uspto-grants-1976_12
Patent number
US04000275

Reaction notes

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