HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1531408Generated: October 30, 2026
4-Methylmorpholine → (R,S)-Benthiavalicarb-isopropyl
https://huagongshe.com/reaction/1531408
Participants
| Role | Name | HCID | Charge |
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| Reactant | 4-Methylmorpholine | HCID 7972 | — |
| Reactant | Isobutyl chloroformate | HCID 62365 | — |
| Reactant | (2R)-3-methyl-2-{[(propan-2-yloxy)carbonyl]amino}butanoic acid | HCID 53692456 | — |
| Reactant | (S)-1-(6-fluoro-2-benzothiazolyl)ethylamine p-toluenesulfonate | HCID 86756512 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | (R,S)-Benthiavalicarb-isopropyl | HCID 86756513 | 69.3% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06197969B1 |
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| Source dataset | uspto-grants-2001_03 |
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| ORD ID | ord-3fcd28bad8a14953980d98313f78e473 |
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| Source note | uspto-grants-2001_03 |
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