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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 524031Generated: October 30, 2026

Acryloyl chloride → HCID 72944768, compound

https://huagongshe.com/reaction/524031

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcryloyl chlorideHCID 13140—
ReactantHCID 86713561HCID 86713561—
SolventDichloromethaneHCID 6344—
ProductHCID 72944768HCID 72944768—

Reaction Conditions

Temperature0 °C

Reaction Steps

2-(2-amino-6-methylphenylamino)-6-(2,6-dichloro-3,5-dimethoxyphenyl)-8-methylpyrido[2,3-d]pyrimidin-7(8H)-one (11) was taken up in DCM (2 ml) and cooled to 0° C., followed by addition of acryloyl chloride (0.010 mL, 0.13 mmol). The reaction was allowed to warm to room temperature and stirred overnight. The mixture was loaded directly onto silica gel and purified by flash chromatography using 0-100% EtOAc/Hexanes gradient to provide the product, N-(2-((6-(2,6-dichloro-3,5-dimethoxyphenyl)-8-methyl-7-oxo-7,8-dihydropyrido[2,3-d]pyrimidin-2-yl)amino)-3-methylphenyl)acrylamide (Compound E). The product was obtained as an off-white solid (10 mg; 19% yield). MS (ES+) C26H23Cl2N5O4, 540 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09340514B2
Source datasetuspto-grants-2016_05
ORD IDord-1a3d0eec46ac4f0ba6ec824246d5a758
Source noteuspto-grants-2016_05