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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 494714Generated: October 31, 2026

Chloroacetaldehyde → HCID 21866997, compound

https://huagongshe.com/reaction/494714

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 chloroacetaldehyde 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). MS APCI (−) m/z 382, 384, 386 (M-, Cl, Br pattern) detected. 1H NMR (400 MHz, CD3OD) δ 8.86 (s, 1H), 7.85 (s, 1H), 7.53 (s, 2H), 7.32 (d, 1H), 6.82 (t, 1H). 19F NMR (376 MHz, CD3OD)−148.3 (s).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07538120B2
Source datasetuspto-grants-2009_05
ORD IDord-fab971988a214c8795abe4fbd749dbfd
Source noteuspto-grants-2009_05