HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1531406Generated: October 31, 2026
4-Methylmorpholine → 1-Methylethyl N-[(1R)-1-[[[(1R)-1-(6-fluoro-2-benzothiazolyl)ethyl]amino]carbonyl]-2-methylpropyl]carbamate
https://huagongshe.com/reaction/1531406
Participants
| Role | Name | HCID | Charge |
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| Reactant | 4-Methylmorpholine | HCID 7972 | — |
| Reactant | Isobutyl chloroformate | HCID 62365 | — |
| Reactant | (R)-1-(6-fluoro-2-benzothiazolyl)ethylamine p-toluenesulfonate | HCID 51350477 | — |
| Reactant | (2R)-3-methyl-2-{[(propan-2-yloxy)carbonyl]amino}butanoic acid | HCID 53692456 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 1-Methylethyl N-[(1R)-1-[[[(1R)-1-(6-fluoro-2-benzothiazolyl)ethyl]amino]carbonyl]-2-methylpropyl]carbamate | HCID 24848546 | 62.7% |
Reaction Steps
In 500 ml of toluene, 10.2 g (0.05 mol) of N-isopropoxycarbonyl-D-valine was dissolved. Thereto were dropwise added, at −5° C., 12.4 g (0.0125 mol) of N-methylmorpholine and 6.8 g (0.05 mol) of isobutyl chlorocarbonate. Thereto was added, at −5° C., 18.3 g (0.05 mol) of (R)-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 suspension of a solid in toluene was filtered to collect the solid. The solid was subjected to Soxhlet extraction for 1 week, and the extract was concentrated to obtain a solid. The solid was recrystallized from xylene to obtain 11.6 g (yield: 62.7%) of isopropyl {(R)-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-84d0880a1b47425fafb940ac0b33cb0d |
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| Source note | uspto-grants-2001_03 |
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