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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1531408Generated: October 30, 2026

4-Methylmorpholine → (R,S)-Benthiavalicarb-isopropyl

https://huagongshe.com/reaction/1531408

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-MethylmorpholineHCID 7972—
ReactantIsobutyl chloroformateHCID 62365—
Reactant(2R)-3-methyl-2-{[(propan-2-yloxy)carbonyl]amino}butanoic acidHCID 53692456—
Reactant(S)-1-(6-fluoro-2-benzothiazolyl)ethylamine p-toluenesulfonateHCID 86756512—
SolventTolueneHCID 1140—
Product(R,S)-Benthiavalicarb-isopropylHCID 8675651369.3%

Reaction Steps

In 250 ml of toluene, 13.4 g (0.066 mol) of N-isopropoxycarbonyl-D-valine was dissolved. Thereto was added 14.3 g (0.144 mol) of N-methylmorpholine. Then was dropwise added at −10° C., 8.6 g (0.063 mol) of isobutyl chlorocarbonate. Thereto was added 22 g (0.06 mol) of (S)-1-(6-fluoro-2-benzothiazolyl)ethylamine p-toluenesulfonate. A reaction and a post-treatment were conducted in the same manner as in Reference Example 1, and the hot toluene solution was filtered in a hot state to remove the insoluble matter. The filtrate was cooled, whereby crystals were precipitated. The crystals were collected by filtration and dried to obtain 15.8 g (yield: 69.3%) of isopropyl {(R)-1-[(S)-1-(6-fluorobenzothiazol-2-yl)ethylcarbamoyl]-2-methylpropyl}carbamate. The compound obtained was confirmed for the structure by IR analysis and NMR analysis in comparison with its authentic material and identified.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06197969B1
Source datasetuspto-grants-2001_03
ORD IDord-3fcd28bad8a14953980d98313f78e473
Source noteuspto-grants-2001_03