HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → HCID 178444647, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | HCID 178444646 | HCID 178444646 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 178444647 | HCID 178444647 | — |
Reaction Steps
To a solution of (2S,3S)-2-[Nα -[N-[N-methyl-N-{2-(N-thiomorpholinocarbonyl-N-methylamino)ethyl}aminocarbonyl]-L-phenylalanyl]-Nα -methyl-L-histidyl]amino-1-cyclohexyl-3-hydroxy-6-methylheptane (300 mg) in ethanol (3 ml), which was cooled to 0° C., was added a solution of 4M hydrogen chloride in ethyl acetate (0.100 ml). After being stirred at the same temperature for 10 minutes, the solution was concentrated in vacuo to give (2S,3S)-2-[Nα -[N-[N-methyl-{2-(N-thiomorpholinocarbonyl-N-methylamino)ethyl}aminocarbonyl]-L-phenylalanyl]-Nα -methyl-L-histidyl]amino-1-cyclohexyl-3-hydroxy-6-methylheptane hydrochloride (310 mg) as an amorphous powder. Rf: 0.38 (10% methanol in chloroform)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05491132 |
| Source dataset | uspto-grants-1996_02 |
| ORD ID | ord-c41d1f89eef140378d75b189ca7d116f |
| Source note | uspto-grants-1996_02 |