HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 847320Generated: October 30, 2026
Potassium Carbonate → HCID 178448276, compound
https://huagongshe.com/reaction/847320
Participants
| Role | Name | HCID | Charge |
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| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | Benzyl [amino(methylsulfanyl)methylene]carbamate | HCID 140362141 | — |
| Reactant | HCID 178448274 | HCID 178448274 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 178448276 | HCID 178448276 | 80% |
Reaction Steps
0.136 g (0.197 mmol) of t-butyl [(S)-α-[[(S)-1-[[(1S,2S,4S)-6-amino-1-(cyclohexylmethyl)-2-hydroxy-4-isopropylhexyl]carbamoyl]-2-imidazol-4-ylethyl]carbamoyl]phenethyl]carbamate hydrochloride, 0.051 g (0.2 mmol) of benzyl [(methylthio)formimidoyl]carbamate and 0.07 ml (0.34 mmol) of Hunig base in 1 ml of absolute ethanol are stirred at 70° under argon for 3 hours. Thereafter, the reaction mixture is cooled, poured into 2N potassium carbonate solution and extracted with methylene chloride. The methylene chloride extracts are dried over magnesium sulphate and evaporated under reduced pressure. Chromatography of the residue obtained on 2 g of silica gel with a mixture of methylene chloride and isopropanol as the eluting agent yields 0.131 g of benzyl [N-[(3S,5S,6S)-6-[[N-[N-(t-butoxycarbonyl)-3-phenyl-L-alanyl]-L-histidyl]amino]-7-cyclohexyl-5-hydroxy-3-isopropylheptyl]amidino]carbamate as a colourless oil, MS: 831 (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05140011 |
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| Source dataset | uspto-grants-1992_08 |
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| ORD ID | ord-e6ff350380b5413ab73cbabc24b11ea9 |
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| Source note | uspto-grants-1992_08 |
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