HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → HCID 178449996, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | HCID 178453493 | HCID 178453493 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | HCID 178449996 | HCID 178449996 | — |
Reaction Steps
A solution of 32 mg (0.043 mmol) of tert-butyl [2-[[(S)-2-[[(S)-1-[[(1S,2R,3S)-1-(cyclohexylmethyl)-3-cyclopropyl-2,3-dihydroxypropyl]carbamoyl]-2-imidazol-4-ylethyl]carbamoyl]-3-phenylpropyl]sulphonyl]-2-methylpropyl]carbamate in 2 ml of dioxan is treated with 2 ml (4 mmol) of 2N hydrochloric acid in dioxan while cooling with ice and stirred for 1 hour. Subsequently, the solution is lyophilized and there are obtained 30 mg of (S)-α-[(S)-α-[[[(2-amino-1,1-dimethylethyl)sulphonyl]methyl]hydrocinnamamido]-N-[(1S,2R,3S)-1-(cyclohexylmethyl)-3-cyclopropyl-2,3-dihydroxypropyl]imidazole-4-propionamide dihydrochloride as a colourless powder; MS: 646 (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05688946 |
| Source dataset | uspto-grants-1997_11 |
| ORD ID | ord-132d206707204d62993bf44bb34a2b67 |
| Source note | uspto-grants-1997_11 |