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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2063319Generated: November 2, 2026

Formic Acid → (9aS)-8-azetidin-3-ylhexahydropyrazino[2,1-c][1,4]oxazin-4(3H)-one

https://huagongshe.com/reaction/2063319

Reaction equation

Participants

RoleNameHCIDCharge
ReactantFormic AcidHCID 284—
ReactantAmmonium formateHCID 2723923—
Reactant(9aS)-8-[1-(diphenylmethyl)azetidin-3-yl]hexahydropyrazino-[2,1-c][1,4]oxazin-4(3H)-oneHCID 16124478—
CatalystPalladiumHCID 23938—
SolventEthanolHCID 702—
Product(9aS)-8-azetidin-3-ylhexahydropyrazino[2,1-c][1,4]oxazin-4(3H)-oneHCID 16124476—

Reaction Conditions

Temperature120 °C

Reaction Steps

(9aS)-8-[1-(Diphenylmethyl)azetidin-3-yl]hexahydropyrazino-[2,1-c][1,4]oxazin-4(3H)-one (85 mg, 0.22 mmol) was dissolved in ethanol (18 mL). The solution was transferred to a 25 mL vial, which contained ethanol (2 mL), 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)-8-azetidin-3-ylhexahydropyrazino[2,1-c][1,4]oxazin-4(3H)-one was used in the next step without purification and quantification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08288370B2
Source datasetuspto-grants-2012_10
ORD IDord-02720b6636034bc5a193337f120f8bf1
Source noteuspto-grants-2012_10