Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Methyl D-valinate hydrochloride | HCID 11984198 | — |
| Reactant | 2-Chloro-1,3-benzothiazole-6-sulfonyl chloride | HCID 12350870 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 86586416 | HCID 86586416 | — |
Reaction Steps
(D)-valine methylester hydrochloride (0.33 g, 2.0 mmol) was dispersed in dichloromethane (5 mL) and cooled down to 0° C. 2-Chloro-6-benzthiazolsulfonyl chloride (0.5 g, 1.0 equi.) prepared in Example 13 was dissolved in dichloromethane (3 mL) to give a dichloromethane solution. Triethylamine (0.83 mL, 3 equi.) and the dichloromethane solution were added while maintaining the temperature of 0° C. When starting material was exhausted after 5 hours, the organic phase was washed with 1N HCl, dried over MgSO4 and distilled under reduced pressure. Then, the product was eluted and purified on silica gel chromatography using ethylacetate/n-hexane (1/3) solvent to prepare the titled compound, (2R)-3-methyl-2-[(2-chlorobenzthiazol-6-sulfonyl)amino] butanoic acid methylester (0.65 g, 90%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06548667B2 |
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| Source dataset | uspto-grants-2003_04 |
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| ORD ID | ord-2fcb8cf0301d44f685c8860be91a6c97 |
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| Source note | uspto-grants-2003_04 |
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