HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 36797Generated: October 30, 2026
Pyridine → Methyl 5-ethylsulfonylamino-2-fluorocarbanilate
https://huagongshe.com/reaction/36797
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Pyridine | HCID 1049 | — |
| Reactant | Methyl chloroformate | HCID 6586 | — |
| Reactant | Ethanesulfonamide, N-(3-amino-4-fluorophenyl)- | HCID 11138584 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | Methyl 5-ethylsulfonylamino-2-fluorocarbanilate | HCID 19937927 | 96.4% |
Reaction Steps
22.1 g (229 mmol) of methyl chloroformate was added dropwise to a mixture of 50.0 g (229 mmol) of N-(3-amino-4-fluorophenyl)ethanesulfonamide, 18.1 g (229 mmol) of pyridine and 500 ml of dichloromethane at a temperature of not higher than 5° C. Thereafter the temperature was raised to room temperature and the reaction was continued for 5 hours. After the dichloromethane layer was separated out by adding water to the resultant mixture, the dichloromethane layer was washed with saturated saline solution and dried over anhydrous sodium sulfate. Thereafter the dichloromethane was distilled off to obtain the crude product (crystals). The crude product was washed with diisopropyl ether, thereby obtaining 61.0 g of the objective product (yield: 96%) in the form of light brown crystals.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05416236 |
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| Source dataset | uspto-grants-1995_05 |
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| ORD ID | ord-d060b7fa82df49f8b9290ad0cf81f7a2 |
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| Source note | uspto-grants-1995_05 |
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