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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 917023Generated: October 28, 2026

Chloroacetaldehyde → HCID 21866982, compound

https://huagongshe.com/reaction/917023

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChloroacetaldehydeHCID 33—
ReactantHCID 68859908HCID 68859908—
SolventEthanolHCID 702—
SolventEthyl AcetateHCID 8857—
ProductHCID 21866982HCID 2186698233%

Reaction Conditions

Temperature80 °C

Reaction Steps

Chloroacetaldehyde (12 μL, 0.188 mmol) was added to a mixture of 6-amino-4-(4-bromo-2-chlorophenylamino)-nicotinic acid tert-butyl ester (42) (50 mg, 0.125 mmol) in EtOH (630 μL). After stirring the reaction mixture at 80° C. for 5 hours, an additional 12 μL of chloroacetaldehyde were added and heating was continued for 10 hours. The reaction mixture was cooled to room temperature and diluted with EtOAc to give a cloudy semi-solution. The organic layer was washed with water, saturated NaHCO3 and brine. The organic layer contains a precipitate, which was collected by filtration to give the desired product (43) (15 mg, 33%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07271178B2
Source datasetuspto-grants-2007_09
ORD IDord-e79fe4195f124c5c988f0b8e6bda03b5
Source noteuspto-grants-2007_09