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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1372712Generated: October 26, 2026

Dimethylformamide → HCID 58778584, compound

https://huagongshe.com/reaction/1372712

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
ReactantTriethylamineHCID 8471—
ReactantOxalyl chlorideHCID 65578—
ReactantEthyl 4-amino-5-chloro-2-fluorophenylacetateHCID 17858807—
Reactant4-Fluoro-1-methyl-1h-indole-3-carboxylic acidHCID 18385290—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
ProductHCID 58778584HCID 5877858452%

Reaction Steps

To a suspension of 4-fluoro-1-methylindole-3-carboxylic acid (700 mg, 3.62 mmol) and DMF (28.0 μl, 0.36 mmol) in methylene chloride (20 ml) was added oxalyl chloride (0.35 ml, 3.99 mmol) in portions under stirring at room temperature. After the reaction mixture was stirred at room temperature for 50 minutes, oxalyl chloride (30 μl) was added, and the mixture was stirred for further 40 minutes. To the reaction mixture, a solution of ethyl (4-amino-5-chloro-2-fluorophenyl)acetate (839 mg, 3.62 mmol) and triethylamine (1.52 ml, 10.9 mmol) in methylene chloride (5 ml) was added and the mixture was heated under reflux at room temperature for 4 hours. After cooling to room temperature, the reaction mixture was added with water, followed by extraction with chloroform. The extract was washed with brine, dried over anhydrous sodium sulfate, and distilled under reduced pressure to remove the solvent. The residue was purified by chromatography opn a silica gel column, whereby from n-hexane-ethyl acetate (2:1, v/v) eluate fractions, ethyl (5-chloro-2-fluoro-4-((4-fluoro-1-methyl-3-indolylcarbonyl)amino)phenyl)acetate (762 mg, 52%) was obtained as a yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07157487B2
Source datasetuspto-grants-2007_01
ORD IDord-9ef4e488fa0941d596f58d7f864149ad
Source noteuspto-grants-2007_01