HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1748260Generated: October 31, 2026
Hydrochloric Acid → trans-3,4-Dimethyl-1-oxo-1,2,3,4-tetrahydropyrazino[1,2-a]indole-7-carboxylic acid
https://huagongshe.com/reaction/1748260
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Ethyl trans-3,4-dimethyl-1-oxo-1,2,3,4-tetrahydropyrazino[1,2-a]indole-7-carboxylate | HCID 86682387 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | trans-3,4-Dimethyl-1-oxo-1,2,3,4-tetrahydropyrazino[1,2-a]indole-7-carboxylic acid | HCID 67235436 | 94.6% |
Reaction Steps
To a suspension of ethyl trans-3,4-dimethyl-1-oxo-1,2,3,4-tetrahydropyrazino[1,2-a]indole-7-carboxylate (930 mg, 3.2 mmol) in ethanol (40 mL) is added 1M NaOH solution (10 mL, 10 mmol). The reaction mixture is heated at 80° C. for 1 h and then cooled to room temperature. The reaction mixture is acidified using concentrated HCl and ethanol is removed under vacuum. The resulting solid is filtered, rinsed with water and dried to afford the title compound (782 mg, 93%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US09150577B2 |
|---|
| Source dataset | uspto-grants-2015_10 |
|---|
| ORD ID | ord-81d043db83904b2aa9d229269ecccc2f |
|---|
| Source note | uspto-grants-2015_10 |
|---|