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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1774645Generated: November 1, 2026

Acryloyl chloride → (S)-N-(1-(6-(5-bromo-1-methyl-2-oxo-1,2-dihydropyridin-3-ylamino)pyridin-2-yloxy)propan-2-yl)acrylamide

https://huagongshe.com/reaction/1774645

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcryloyl chlorideHCID 13140—
Reactant(S)-3-(6-(2-aminopropoxyl)pyridin-2-ylamino)-5-bromo-1-methylpyridin-2(1H)-one hydrochlorideHCID 118117014—
SolventDichloromethaneHCID 6344—
Product(S)-N-(1-(6-(5-bromo-1-methyl-2-oxo-1,2-dihydropyridin-3-ylamino)pyridin-2-yloxy)propan-2-yl)acrylamideHCID 11811648570%

Reaction Steps

To an ice-cooled mixture of 107c (390 mg, 1.0 mmol) and TEA (0.53 ml, 3.0 mmol) in DCM (20 mL) was added acryloyl chloride (0.23 ml, 2.0 mmol) dropwise. The reaction mixture was stirred at rt for 2 h and quenched with water. The organic layer was separated, dried over Na2SO4, filtered and concentrated. The residue was purified by silica gel chromatography (DCM/MeOH=10/1) to give 107d (284 mg, 70%) as brown solid. MS-ESI: [M+H]+ 409.0

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09260415B2
Source datasetuspto-grants-2016_02
ORD IDord-7dde1bb3de2c46bf9a77bdafa2c58993
Source noteuspto-grants-2016_02