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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1369138Generated: October 31, 2026

Hydrochloric Acid → Benthiavalicarb isopropyl

https://huagongshe.com/reaction/1369138

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantL-ValineHCID 6287—
ReactantIsopropyl chloroformateHCID 7917—
ReactantSodium HydroxideHCID 14798—
Reactant(R)-1-(6-Fluorobenzo[D]thiazol-2-YL)ethanamineHCID 10921462—
CatalystN,N-dimethylaminobenzylamineHCID 86587301—
SolventWaterHCID 962—
SolventTolueneHCID 1140—
ProductBenthiavalicarb isopropylHCID 5329738192.4%

Reaction Steps

16.1 g (0.092 mole) of 23% sodium hydroxide, 10 ml of water and 4.7 g (0.04 mole) of L-valine were placed in a 300-ml reaction flask, and stirred at room temperature for 30 minutes. Thereto was dropwise added 5.9 g.(0.048 mole) of isopropyl chlorocarbonate at room temperature, followed by stirring for 1 hour. The resulting mixture was neutralized with concentrated hydrochloric acid. Thereto were added 50 ml of toluene and 0.06 g (0.0004 mole) of N,N-dimethylaminobenzylamine. Then, 4.7 g (0.038 mole) of isopropyl chlorocarbonate was added dropwise at room temperature, followed by stirring for 1 hour. Thereafter, there was dropwise added a solution of 7.5 g (0.038 mole) of (R)-1-(6-fluorobenzothiazol-2-yl)ethylamine (purity: 98.3%, optical purity: 99.0% ee) dissolved in 50 ml of toluene, produced according to the above Reference Example, followed by stirring at room temperature for 2 hours. 50 ml of water was added; the resulting mixture was heated to 70° C. and subjected to phase separation; the toluene layer was washed with 50 ml of hot water and subjected to solvent removal to obtain 13.4 g (yield: 92.4%) of isopropyl [(S)-1-[(R)-1(6-fluorobenzothiazol-2-yl)ethylcarbamoyl]-2-methylpropyl]carbamate (purity: 96.3%, the proportion of formed intended substance in four diastereomers: 98.5%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06576765B2
Source datasetuspto-grants-2003_06
ORD IDord-2a5436161bb9463b938f144aeabb85a9
Source noteuspto-grants-2003_06