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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1627467Generated: October 25, 2026

Isopropyl chloroformate → N-[[1-[(2-Furanylcarbonyl)amino]cyclohexyl]carbonyl]-L-valinol

https://huagongshe.com/reaction/1627467

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIsopropyl chloroformateHCID 7917—
ReactantTriethylamineHCID 8471—
ReactantSodium borohydrideHCID 4311764—
ReactantN-[[1-[(2-furanylcarbonyl)amino]cyclohexyl]carbonyl]-L-valineHCID 24737720—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
SolventEthyl AcetateHCID 8857—
ProductN-[[1-[(2-Furanylcarbonyl)amino]cyclohexyl]carbonyl]-L-valinolHCID 2487608716%

Reaction Conditions

Temperature0 °C

Reaction Steps

Under an argon atmosphere, 72 mg (0.59 mmol) of isopropyl chlorocarbonate was added to a solution of 200 mg (0.59 mmol) of N-[[1-[(2-furanylcarbonyl)amino]cyclohexyl]carbonyl]-L-valine and 60 mg (0.59 mmol) of triethylamine in 2 ml of tetrahydrofuran under ice-cooling. After the mixture was stirred at 0° C. for 2 hours, the reaction solution was filtered and poured to a solution of 45 mg (1.2 mmol) of sodium borohydride in 1 ml of water, and the mixture was stirred overnight. Ethyl acetate was added to the reaction solution, and the mixture was successively washed with a 10% aqueous potassium hydrogensulfate solution, a saturated aqueous sodium hydrogencarbonate solution and saturated brine, followed by drying with sodium sulfate. After the solvent was distilled off under reduced pressure, the obtained crystal was washed with ether to obtain 30 mg (16%) of the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08785631B2
Source datasetuspto-grants-2014_07
ORD IDord-f6484c0539f7410fa554503a782cdb29
Source noteuspto-grants-2014_07