HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 397670Generated: October 26, 2026
Methanol → methyl (2S)-1-[(4-fluorophenyl)sulfonyl]-2-piperidinecarboxylate
https://huagongshe.com/reaction/397670
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methanol | HCID 887 | — |
| Reactant | (2S)-1-[(4-fluorophenyl)sulfonyl]-2-piperidinecarboxylic acid | HCID 768662 | — |
| Reactant | 1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochloride | HCID 2723939 | — |
| Catalyst | 4-(Dimethylamino)pyridine | HCID 14284 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | methyl (2S)-1-[(4-fluorophenyl)sulfonyl]-2-piperidinecarboxylate | HCID 57268970 | 79.4% |
Reaction Steps
4-Dimethylaminopyridine (61 mg), methanol (45 μl) and 1-(3-dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride (192 mg) were added to a solution of (2S)-1-[(4-fluorophenyl)sulfonyl]-2-piperidinecarboxylic acid (287 mg) [see Preparation 38] in dichloromethane (6 ml). The reaction mixture was stirred at room temperature for 56 hours after which time it was diluted with dichloromethane and washed with 1N aqueous hydrochloric acid solution followed by saturated aqueous sodium hydrogen carbonate solution. The organic layer was dried over magnesium sulphate and the solvent removed under reduced pressure. The crude product was purified by column chromatography on silica gel eluting with a solvent gradient of 90:10 changing to 50:50, by volume, hexane:ethyl acetate, to afford methyl (2S)-1-[(4-fluorophenyl)sulfonyl]-2-piperidinecarboxylate (239 mg) as an oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US06610707B1 |
|---|
| Source dataset | uspto-grants-2003_08 |
|---|
| ORD ID | ord-9a4492d48a8047608dbd2a1c2e630d4f |
|---|
| Source note | uspto-grants-2003_08 |
|---|