Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | HCID 86753112 | HCID 86753112 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 86753110 | HCID 86753110 | — |
Reaction Steps
Under ice cooling, a hydrochloric acid gas was passed through a stirred solution of 6.79 g of ethyl 3-[3-(2-t-butoxycarbonyl-1,2,3,4-tetrahydro-3-isoquinolinyl)-carbonylamino-2,3-dihydro-2-oxo-1-pentyl-1H-indol-3-yl]-propionate in ethyl acetate (75 ml) until the gas was saturated. The mixture was stirred at 0° C. for 2.5 hours. After removal of solvent, the residue was triturated in isopropyl ether to afford 6.05 g of ethyl 3-[2,3-dihydro-2-oxo-1-pentyl-3-(1,2,3,4-tetrahydro-3-isoquinolinyl)-carbonylamino-1H-indol-3-yl]propionate hydrochloride as a pale yellow amorphous solid. IR (Nujol) (cm-1): 3180, 1725, 1690, 1610, FAB-MS (m/z): 478 (MH+), 132 (base).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US05807883 |
|---|
| Source dataset | uspto-grants-1998_09 |
|---|
| ORD ID | ord-8f66ae57a72440fcbc5269f7502ab010 |
|---|
| Source note | uspto-grants-1998_09 |
|---|