HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1627467Generated: October 25, 2026
Isopropyl chloroformate → N-[[1-[(2-Furanylcarbonyl)amino]cyclohexyl]carbonyl]-L-valinol
https://huagongshe.com/reaction/1627467
Participants
| Role | Name | HCID | Charge |
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| Reactant | Isopropyl chloroformate | HCID 7917 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | N-[[1-[(2-furanylcarbonyl)amino]cyclohexyl]carbonyl]-L-valine | HCID 24737720 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | N-[[1-[(2-Furanylcarbonyl)amino]cyclohexyl]carbonyl]-L-valinol | HCID 24876087 | 16% |
Reaction Steps
Under an argon atmosphere, 72 mg (0.59 mmol) of isopropyl chlorocarbonate was added to a solution of 200 mg (0.59 mmol) of N-[[1-[(2-furanylcarbonyl)amino]cyclohexyl]carbonyl]-L-valine and 60 mg (0.59 mmol) of triethylamine in 2 ml of tetrahydrofuran under ice-cooling. After the mixture was stirred at 0° C. for 2 hours, the reaction solution was filtered and poured to a solution of 45 mg (1.2 mmol) of sodium borohydride in 1 ml of water, and the mixture was stirred overnight. Ethyl acetate was added to the reaction solution, and the mixture was successively washed with a 10% aqueous potassium hydrogensulfate solution, a saturated aqueous sodium hydrogencarbonate solution and saturated brine, followed by drying with sodium sulfate. After the solvent was distilled off under reduced pressure, the obtained crystal was washed with ether to obtain 30 mg (16%) of the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08785631B2 |
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| Source dataset | uspto-grants-2014_07 |
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| ORD ID | ord-f6484c0539f7410fa554503a782cdb29 |
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| Source note | uspto-grants-2014_07 |
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