HuagongsheHuagongshe Chemistry Print Report · For research reference only
HCID 178431645, compound → HCID 178455619, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | HCID 178431645 | HCID 178431645 | — |
| Solvent | Hydrochloric Acid | HCID 313 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 178455619 | HCID 178455619 | 6.7% |
Reaction Steps
A solution of 90 mg (0.3 mmol) of (S)-α-[(S)-α-[(tert-butylsulphonyl)methyl]hydrocinnamamido]-N-[(S)-1-[(4R,5S)-5-cyclopropyl-2,2-dimethyl-1,3-dioxolan-4-yl]-2-(4-oxocyclohexyl)ethyl]imidazole-4-propionamide in 1 ml of methanol and 1 ml of 2N hydrochloric acid is stirred at room temperature for 3 hours. Subsequently, the reaction solution is evaporated and, for purification, the residue is chromatographed on 20 g of silica gel using a 14:1:0.1 mixture of methylene chloride, methanol and ammonia as the eluent. There are obtained 13 mg of (S)-α-[(S)-α-[(tert-butylsulphonyl)methyl]hydrocinnamamido]-N-[(1S,2R,3S)-3-cyclopropyl-2,3-dihydroxy-1-[(4-oxocyclohexyl)methyl]propyl]imidazole-4-propionamide as a colourless solid; MS: 684 (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05688946 |
| Source dataset | uspto-grants-1997_11 |
| ORD ID | ord-1c763452eb784446a0deab2fb10fe344 |
| Source note | uspto-grants-1997_11 |