Ethyl bromoacetate → HCID 86585745, compound

HRID 1281126Notes

Reaction equation

HRID 1281126 reaction equation
[Cl:1][C:2]1[C:18]([Cl:19])=[CH:17][C:5]2[N:6]=[C:7]([C:9]3[CH:14]=[CH:13][C:12]([CH:15]=[O:16])=[CH:11][CH:10]=3)[NH:8][C:4]=2[CH:3]=1.Br[CH2:21][C:22]([O:24][CH2:25][CH3:26])=[O:23]>>[Cl:19][C:18]1[C:2]([Cl:1])=[CH:3][C:4]2[N:8]([CH2:21][C:22]([O:24][CH2:25][CH3:26])=[O:23])[C:7]([C:9]3[CH:10]=[CH:11][C:12]([CH:15]=[O:16])=[CH:13][CH:14]=3)=[N:6][C:5]=2[CH:17]=1

Participants

3

Reactant 2

HCID 7748Ethyl bromoacetateHCID 184267935,6-Dichloro-2-(4-formylphenyl)benzimidazole

Product 1

HCID 86585745HCID 86585745, compound

Procedure

Ethyl [5,6-dichloro2-(4-formylphenyl)benzimidazol-1-yl]acetate was prepared from 5,6-dichloro-2-(4-formylphenyl)benzimidazole obtained in Example 13 and ethyl bromoacetate by following General Procedure 3.

Sources & evidence

ORD record
ord-953cea9e89474e1a8191263e291303af
Source dataset
uspto-grants-2002_09
Patent number
US06452014B1

Reaction notes

Loading…