HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 857892Generated: October 30, 2026
Hydrogen Peroxide → HCID 68887618, compound
https://huagongshe.com/reaction/857892
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrogen Peroxide | HCID 784 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Sodium Thiosulfate | HCID 24477 | — |
| Reactant | HCID 68888191 | HCID 68888191 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 68887618 | HCID 68887618 | — |
Reaction Steps
A solution of 8-cyano-6-phenyl-3,4-dihydro-1H-pyrrolo[1,2-a]pyrazine-2-carboxylic acid tert-butyl ester (3.87 g, Reference Example 4(a)) in methanol (200 mL) was treated with a 10M aqueous solution of sodium hydroxide (10.45 mL), then with a 27.5% w/w aqueous solution of hydrogen peroxide (0.74 mL). After stirring at 50° C. for 0.75 hour the reaction mixture was further treated with a 27.5% w/w aqueous solution of hydrogen peroxide (0.74 mL). After further stirring at 50° C. for 2 hours the reaction mixture was then further treated with a 27.5% w/w aqueous solution of hydrogen peroxide (0.74 mL). After further stirring at 50° C. for 1.5 hours the reaction mixture was allowed to cool to room temperature and treated with a saturated aqueous solution of sodium thiosulfate (20 mL). After stirring at room temperature for 15 minutes the reaction mixture was evaporated and then treated with ethyl acetate (650 mL) and water (150 mL). The organic phase was separated, washed with water (150 mL) and then dried over sodium sulfate. The organic phase was then evaporated to give the title compound (4.06 g) as a white solid, m.p. 208–210° C. MS: 342 [MH]+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07148215B2 |
|---|
| Source dataset | uspto-grants-2006_12 |
|---|
| ORD ID | ord-9092977c1c724eddae19117d14549001 |
|---|
| Source note | uspto-grants-2006_12 |
|---|