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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 351907Generated: October 30, 2026

Hydrochloric Acid → HCID 22714681, compound

https://huagongshe.com/reaction/351907

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantTriethylamineHCID 8471—
Reactant2-FluoroanilineHCID 9584—
ReactantEthyl chloroformateHCID 10928—
Reactant4-Oxo-4,5,6,7-tetrahydro-1H-indole-3-carboxylic acidHCID 15337632—
SolventDimethylformamideHCID 6228—
ProductHCID 22714681HCID 2271468164.9%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution of 4-oxo-4,5,6,7-tetrahydro-1H-indole-3-carboxylic acid (538 mg, 3 mmol) and triethylamine (0.88 mL, 6.3 mmol) in N,N-dimethylformamide (15 mL) at 0° C. was added ethyl chloroformate (0.57 mL, 6 mmol). After stirring at 0° C. for 45 minutes, 2-fluoroaniline (0.58 mL, 6 mmol) wad added. The mixture was stirred for an additional 45 minutes, then allowed to stir at ambient temperature for 14 hours. The mixture was poured into aqueous 1.2 N hydrochloric acid and extracted 2× with ethyl acetate. The combined organic layers were washed with water, dried over magnesium sulfate, filtered, and concentrated in vacuo. To the residue was added aqueous 1N sodium hydroxide (10 mL) and ethyl alcohol (2 mL) and the mixture heated at reflux for 4.5 hours. After cooling in an ice water bath, the mixture was acidified with aqueous hydrochloric acid, the precipitate collected, rinsed with water and dried. Recrystallization from ethyl alcohol afforded N-(2-fluorophenyl)-4-oxo-4,5,6,7-tetrahydro-1H-indole-3-carboxamide (Compound 46)(530 mg). mp 238-240° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06743817B2
Source datasetuspto-grants-2004_06
ORD IDord-30b41385a3314ed191abcff9d5a37876
Source noteuspto-grants-2004_06