HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 582841Generated: October 30, 2026
Hydrochloric Acid → HCID 22714681, compound
https://huagongshe.com/reaction/582841
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 2-Fluoroaniline | HCID 9584 | — |
| Reactant | Ethyl chloroformate | HCID 10928 | — |
| Reactant | 4-Oxo-4,5,6,7-tetrahydro-1H-indole-3-carboxylic acid | HCID 15337632 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 22714681 | HCID 22714681 | 64.9% |
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 1.2N 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05925770 |
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| Source dataset | uspto-grants-1999_07 |
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| ORD ID | ord-cce8cd52c6c24913830b4f192ca36e76 |
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| Source note | uspto-grants-1999_07 |
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