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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 857509Generated: November 1, 2026

Chloroacetaldehyde → HCID 21866997, compound

https://huagongshe.com/reaction/857509

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChloroacetaldehydeHCID 33—
ReactantHCID 68860780HCID 68860780—
SolventEthanolHCID 702—
ProductHCID 21866997HCID 2186699774%

Reaction Conditions

Temperature70 °C

Reaction Steps

Chloroacetaldehyde (23 μL, 0.360 mmol) was added to a mixture of 6-amino-4-(4-bromo-2-chlorophenylamino)-5-fluoronicotinic acid tert-butyl ester (45) (75 mg, 0.180 mmol) in EtOH (1 mL). After stirring the reaction mixture at 70° C. for 10 hours, an additional 10 μL chloro-acetaldehyde was added and heating was continued for 33 hours. The reaction mixture was cooled to room temperature and desired product (46) was collected by filtration. The filtrate was diluted with EtOAc and washed with water, saturated NaHCO3 and brine. The organic layer was dried (Na2SO4) and concentrated to give additional product (46) (51 mg, 74% combined recovery).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07144907B2
Source datasetuspto-grants-2006_12
ORD IDord-c6f050772772437f99f6224c5e81acb8
Source noteuspto-grants-2006_12