HCID 558912, compound → HCID 21489213, compound

HRID 1974285Notes

Reaction equation

HRID 1974285 reaction equation
[Cl:1][C:2]1[CH:11]=[C:10]2[C:5]([C:6](=[O:19])[N:7]3[C:14]4[CH:15]=[CH:16][CH:17]=[CH:18][C:13]=4[NH:12][C:8]3=[N:9]2)=[CH:4][CH:3]=1.Br[CH2:21][CH2:22][CH:23]1[O:26][CH:24]1[CH3:25]>>[Cl:1][C:2]1[CH:11]=[C:10]2[C:5]([C:6](=[O:19])[N:7]3[C:14]4[CH:15]=[CH:16][CH:17]=[CH:18][C:13]=4[N:12]([CH2:21][CH2:22][CH:23]4[O:26][CH:24]4[CH3:25])[C:8]3=[N:9]2)=[CH:4][CH:3]=1

Participants

3

Reactant 2

HCID 558912HCID 558912, compoundHCID 178515068HCID 178515068, compound

Product 1

HCID 21489213HCID 21489213, compound

Procedure

3-Chloro-6-(3,4-epoxypentyl)benzimidazo[2,1-b]quinazolin-12(6H)one is prepared with 3-chlorobenzimidazo[2,1-b]quinazolin-12(6H)one and 1-bromo-3,4-epoxypentane.

Sources & evidence

ORD record
ord-328cb8ff92724aaba0f88cc41f7967f3
Source dataset
uspto-grants-1976_12
Patent number
US04000275

Reaction notes

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