HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → Benzyl((5s)-7-[(3-amino-2-hydroxypropyl)amino]-5-{[(benzyloxy)carbonyl]amino}-7-oxoheptyl)carbamate hydrochloride
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | benzyl{(1S)-5-{[(benzyloxy)carbonyl]amino}-1-[2-({3-[(tert-butoxycarbonyl)amino]-2-hydroxypropyl}amino)-2-oxoethyl]pentyl}carbamate | HCID 131727161 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | Benzyl((5s)-7-[(3-amino-2-hydroxypropyl)amino]-5-{[(benzyloxy)carbonyl]amino}-7-oxoheptyl)carbamate hydrochloride | HCID 69219646 | — |
Reaction Steps
11 ml of a 4M solution of hydrogen chloride in dioxane are added to a solution of 160 mg (0.267 mmol) of benzyl{(1S)-5-{[(benzyloxy)carbonyl]amino}-1-[2-({3-[(tert-butoxycarbonyl)amino]-2-hydroxypropyl}amino)-2-oxoethyl]pentyl}carbamate (Example 160A) in 5.5 ml of dioxane at 0° C. The mixture is stirred at RT for 1 h. The reaction solution is concentrated, coevaporated with dichloromethane several times and dried under high vacuum. The crude product is reacted without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07446102B2 |
| Source dataset | uspto-grants-2008_11 |
| ORD ID | ord-3fc73e7a9e9c43728f173b23b7fc075e |
| Source note | uspto-grants-2008_11 |