HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1900177Generated: October 25, 2026
Water → N1-[2-(4-cyanophenoxy)-1-methylethyl]-N2-phenoxythiocarbonyl-L-valinamide
https://huagongshe.com/reaction/1900177
Participants
| Role | Name | HCID | Charge |
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| Reactant | Water | HCID 962 | — |
| Reactant | 4-Methylmorpholine | HCID 7972 | — |
| Reactant | Phenyl thioxochloroformate | HCID 70498 | — |
| Reactant | N1-[2-(4-cyanophenoxy)-1-methylethyl]-L-valinamide | HCID 22866848 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | N1-[2-(4-cyanophenoxy)-1-methylethyl]-N2-phenoxythiocarbonyl-L-valinamide | HCID 54176149 | 75% |
Reaction Steps
0.4 g of N-methyhnorpholine was added to a suspension containing 1.1 g of N1 -[2-(4-cyanophenoxy)-1-methylethyl]-L-valinamide suspended in 40 ml of methylene chloride, at -15° C. After 0.7 g of phenyl chlorothionoformate was added to the mixture at -15° C., the reaction mixture was allowed to sit and warm naturally to room temperature while being stirred, and was stirred for 15 hours at room temperature. Water was subsequently added to the reaction mixture. After the methylene chloride layer was washed with water, the organic layer was dried over anhydrous magnesium sulfate and the methylene chloride was removed under reduced pressure. The residue was purified by column chromatography on silica gel, thus obtaining 1.2 g of the desired product in the form of a yellow glutinous substance (yield: 75%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05574064 |
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| Source dataset | uspto-grants-1996_11 |
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| ORD ID | ord-1898cc8362be43a890087bf1f6bb60cd |
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| Source note | uspto-grants-1996_11 |
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