HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → 2-Benzyloxycarbonylamino-2-methyl-N-[2,3,4,5-tetrahydro-4-oxo-1-[[2'-(aminomethyl)[1,1'-biphenyl]-4-yl]methyl]-1H-naphtho[2,1-b]azepin-3(R)-yl]propanamide, hydrochloride
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | 2-Benzyloxycarbonylamino-2-methyl-N-[2,3,4,5-tetra-hydro-4-oxo-1-[[2'-[(t-butoxycarbonylamino)methyl]-[1,1'-biphenyl]-4-yl]methyl]-1H-naphtho[2,1-b]azepin-3(R)-yl]-propanamide | HCID 20641419 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 2-Benzyloxycarbonylamino-2-methyl-N-[2,3,4,5-tetrahydro-4-oxo-1-[[2'-(aminomethyl)[1,1'-biphenyl]-4-yl]methyl]-1H-naphtho[2,1-b]azepin-3(R)-yl]propanamide, hydrochloride | HCID 131722473 | — |
Reaction Steps
To a solution of of 2-benzyloxycarbonylamino-2-methyl-N-[2,3,4,5-tetrahydro-4-oxo-1-[[2′-[(t-butoxycarbonylamino)methyl][1,1′-biphenyl]-4-yl]methyl]-1H-naphtho[2,1-b]azepin-3(R)-yl]propanamide (Step H) in methanol is added 9N aqueous hydrochloric acid. The reaction mixture is stirred overnight at room temperature then the solvent is removed under vacuum. The resulting oil is dissolved in methanol and the solvent is removed under vacuum to afford the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06211174B1 |
| Source dataset | uspto-grants-2001_04 |
| ORD ID | ord-a1aba9dea2c448f69284bb84b08e3918 |
| Source note | uspto-grants-2001_04 |