HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1531405Generated: October 31, 2026
4-Methylmorpholine → Benthiavalicarb isopropyl
https://huagongshe.com/reaction/1531405
Participants
| Role | Name | HCID | Charge |
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| Reactant | 4-Methylmorpholine | HCID 7972 | — |
| Reactant | Isobutyl chloroformate | HCID 62365 | — |
| Reactant | (2S)-3-methyl-2-(((propan-2-yloxy)carbonyl)amino)butanoic acid | HCID 11063514 | — |
| Reactant | (R)-1-(6-fluoro-2-benzothiazolyl)ethylamine p-toluenesulfonate | HCID 51350477 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | Benthiavalicarb isopropyl | HCID 53297381 | 132.2% |
Reaction Steps
In 500 ml of toluene, 18.9 g (0.093 mol) of N-isopropoxycarbonyl-L-valine was dissolved. The solution was cooled to −5° C. Thereto were dropwise added, at −5° C., 23.0 g (0.233 mol) of N-methylmorpholine and 12.7 g (0.093 mol) of isobutyl chlorocarbonate. Thereto was added, at −5° C., 17.4 g (0.047 mol) of (R)-1-(6-fluoro-2-benzothiazolyl)ethylamine p-toluenesulfonate in one portion. The mixture was stirred at the same temperature for 0.5 hour and then at room temperature for 2 hours. To the reaction mixture was added 300 ml of water. The mixture was heated to 70° C. to dissolve the solid. The toluene layer was separated, washed with hot water, and then cooled, whereby a solid was precipitated. The solid was collected by filtration and dried to obtain 23.7 g (yield: 70%) of isopropyl {(S)-1-[(R)-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-5ef1d0145bbf48adb611dfe184ffa7fe |
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| Source note | uspto-grants-2001_03 |
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