Ethyl chloroacetate → HCID 178472959, compound

Reaction equation

[Br:1][C:2]1[CH:3]=[C:4]2[N:10]=[C:9]([C:11]3[CH:16]=[CH:15][C:14]([OH:17])=[CH:13][CH:12]=3)[NH:8][C:5]2=[N:6][CH:7]=1.Cl[CH2:19][C:20]([O:22][CH2:23][CH3:24])=[O:21]>>[Br:1][C:2]1[CH:3]=[C:4]2[N:10]=[C:9]([C:11]3[CH:12]=[CH:13][C:14]([O:17][CH2:19][C:20]([O:22][CH2:23][CH3:24])=[O:21])=[CH:15][CH:16]=3)[NH:8][C:5]2=[N:6][CH:7]=1

Participants

Reactant 2

HCID 7751Ethyl chloroacetate

HCID 178515890HCID 178515890, compound

Product 1

HCID 178472959HCID 178472959, compound

Procedure

The title compound was prepared from 4-(6-bromo-3H-imidazo[4,5-b]pyridin-2-yl)phenol and ethyl chloroacetate using the method described in Example 41.

Sources & evidence

ORD record: ord-9d86a83f92a74f9fa897b666cb5c51b6
Source dataset: uspto-grants-2008_08
DOI: 10.6084/m9.figshare.5104873.v1
Patent number: US07410966B2

Reaction notes

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