HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2063317Generated: November 2, 2026
Formic Acid → (9AS)-Hexahydropyrazino-[2,1-c][1,4]oxazin-4(3H)-one
https://huagongshe.com/reaction/2063317
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Formic Acid | HCID 284 | — |
| Reactant | Ammonium formate | HCID 2723923 | — |
| Reactant | benzyl (9aS)-4-oxohexahydropyrazino[2,1-c][1,4]oxazine-8(1H)-carboxylate | HCID 16124472 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | (9AS)-Hexahydropyrazino-[2,1-c][1,4]oxazin-4(3H)-one | HCID 16124477 | — |
Reaction Steps
Benzyl (9aS)-4-oxohexahydropyrazino[2,1-c][1,4]oxazine-8(1H)-carboxylate (0.19 g, 0.65 mmol was dissolved in ethanol (20 mL). The solution was transferred to a 25 mL vial, which contained 10% palladium on carbon (0.1 g), formic acid (0.1 g, 2.2 mmol) and ammonium formate (0.2 g, 3.17 mmol). The mixture was heated for 5 min at 120° C. using microwave single node heating. The catalyst was filtered off and the solution of crude (9aS)-hexahydropyrazino[2,1-c][1,4]oxazin-4(3H)-one was used in the next step without purification and quantification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08288370B2 |
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| Source dataset | uspto-grants-2012_10 |
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| ORD ID | ord-ea54da427c924e96b8e39e87b012a42a |
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| Source note | uspto-grants-2012_10 |
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