HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2297716Generated: October 31, 2026
Benzyl chloroformate → HCID 59923462, compound
https://huagongshe.com/reaction/2297716
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Benzyl chloroformate | HCID 10387 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | HCID 59923442 | HCID 59923442 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 59923462 | HCID 59923462 | 69% |
Reaction Steps
(2S)-2-[3-(2-Mercaptoethyl)-3-phenethylureido]-3-phenylpropionic acid (Compound No. 11-1, 108 mg) is dissolved in anhydrous methylene chloride (1.5 ml) under a nitrogen atmosphere, and the solution is stirred. To the solution are added N,N-diisopropylethylamine (0.07 ml) and benzyloxycarbonyl chloride (0.05 ml) successively under ice cooling, and the mixture is stirred at room temperature overnight. The reaction mixture is concentrated under reduced pressure, water is added to the residue, and the whole is extracted with ethyl acetate. The organic layer is washed with a 10% aqueous citric acid solution, water and saturated brine successively, dried over anhydrous sodium sulfate and concentrated under reduced pressure. The resulting oily matter is purified by silica gel column chromatography to give 102 mg (69%) of the titled compound (Compound No. 12-1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06492370B1 |
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| Source dataset | uspto-grants-2002_12 |
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| ORD ID | ord-8c8b909611d1464fb93c864c376d50b4 |
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| Source note | uspto-grants-2002_12 |
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