HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1900189Generated: October 30, 2026
N-Methylpiperidine → HCID 53967854, compound
https://huagongshe.com/reaction/1900189
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | N-Methylpiperidine | HCID 12291 | — |
| Reactant | Isobutyl chloroformate | HCID 62365 | — |
| Reactant | N-Phenoxycarbonyl-L-valine | HCID 9816135 | — |
| Reactant | HCID 18972720 | HCID 18972720 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 53967854 | HCID 53967854 | 18.2% |
Reaction Steps
1.6 g of N-methylpiperidine was added to a solution containing 3.9 g of N-phenoxycarbonyl-L-valine dissolved in 80 ml of methylene chloride, at -20° C. After the mixture was stirred for 10 minutes at the same temperature, 2.2 g of isobutyl chloroformate was added to the mixture, and stirred for 1 hour at -20° C. 3.0 g of 2-(4-fluoro-N-methylanilino)-1-methylethylamine was added to this mixture at -60° C., and then the reaction mixture was allowed to sit and warm naturally to room temperature while being stirred, and was stirred for 20 hours at room temperature. Water was subsequently added to the reaction mixture. After the methylene chloride layer was washed successively with a 5% aqueous solution of sodium bicarbonate and water, the organic layer was dried over anhydrous sodium sulfate and the methylene chloride was removed under reduced pressure. The residue was purified by column chromatography on silica gel, thus obtaining 1.2 g of the desired product in the form of a white crystal (yield: 19%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05574064 |
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| Source dataset | uspto-grants-1996_11 |
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| ORD ID | ord-5b3e4b33978f425db0dcbb3b0cd74112 |
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| Source note | uspto-grants-1996_11 |
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