HuagongsheHuagongshe Chemistry Print Report · For research reference only
Potassium Hydroxide → HCID 14155429, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | HCID 20144288 | HCID 20144288 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 14155429 | HCID 14155429 | — |
Reaction Steps
To a solution of 4.4 g of 1,3,4,16b-tetrahydro-2-ethoxycarbonyl-2H,10H-indolo[2,1-c]pyrazino[1,2-a][1,4]benzodiazepine in 88 ml ethanol is added 24 ml of 50% potassium hydroxide solution. The reaction mixture is heated at reflux temperature for 6 hours. The solvent is evaporated to dryness under reduced pressure and the residue extracted with a mixture of 350 ml of diethyl ether and 250 ml of water. The ethereal extract is washed with water, separated and then dried over anhydrous magnesium sulfate. The solvent is evaporated to yield 1,3,4,16b-tetrahydro-2H,10H-indolo[2,1-c]pyrazino[1,2-a][1,4]benzodiazepine which is converted to the hydrochloride salt, mp 263° dec.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04737496 |
| Source dataset | uspto-grants-1988_04 |
| ORD ID | ord-c97e0cb37f954e3baabf6ba0ff03c8cc |
| Source note | uspto-grants-1988_04 |