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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1773752Generated: October 29, 2026

6-bromo-N,N-dimethylpyridin-2-amine → 4-((6-(dimethylamino)pyridin-2-yl)(hydroxy)(pyridin-2-yl)methyl)-6-(3,5-dimethylisoxazol-4-yl)-1H-benzo[d]imidazol-2(3H)-one

https://huagongshe.com/reaction/1773752

Reaction equation

Participants

RoleNameHCIDCharge
Reactant6-bromo-N,N-dimethylpyridin-2-amineHCID 14006062—
Reactant6-(3,5-dimethylisoxazol-4-yl)-4-(hydroxy(6-methylpyridin-2-yl)(pyridin-2-yl)methyl)-1H-benzo[d]imidazol-2(3H)-oneHCID 86297160—
Product4-((6-(dimethylamino)pyridin-2-yl)(hydroxy)(pyridin-2-yl)methyl)-6-(3,5-dimethylisoxazol-4-yl)-1H-benzo[d]imidazol-2(3H)-oneHCID 117601948—

Reaction Steps

A procedure similar to that used for 6-(3,5-dimethylisoxazol-4-yl)-4-(hydroxy(6-methylpyridin-2-yl)(pyridin-2-yl)methyl)-1H-benzo[d]imidazol-2(3H)-one, using 6-bromo-2-N,N-dimethylaminopyridine as the starting material was used to produce the intermediate (C32H36N6O5, 585.2 (M+1)), which was taken directly to the deprotection step to yield the title compound as a yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09255089B2
Source datasetuspto-grants-2016_02
ORD IDord-25971bb939fc490280371bcdeb585635
Source noteuspto-grants-2016_02