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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1054184Generated: November 3, 2026

Ethyl Acetate → AZD9977

https://huagongshe.com/reaction/1054184

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcetateHCID 8857—
ReactantDiisopropylethylamineHCID 81531—
ReactantPropylphosphonic anhydrideHCID 111923—
Reactant3-Oxo-3,4-dihydro-2H-1,4-benzoxazine-6-carboxylic acidHCID 706121—
Reactant2-[(3S)-7-Fluoro-3,4-dihydro-2H-1,4-benzoxazin-3-yl]-N-methyl-acetamideHCID 118599775—
SolventWaterHCID 962—
SolventButyl AcetateHCID 31272—
ProductAZD9977HCID 11859972750.9%

Reaction Conditions

Temperature80 °C

Reaction Steps

3-Oxo-3,4-dihydro-2H-1,4-benzoxazine-6-carboxylic acid (9.58 g, 48.0 mmol) was suspended with stirring in n-butyl acetate (48 mL). T3P in ethyl acetate (52.5 mL, 87.5 mmol, 50.0% w/w) was added followed by DIPEA (3.82 mL, 21.9 mmol). The resulting suspension was heated at 80° C. over night. 2-[(3S)-7-fluoro-3,4-dihydro-2H-1,4-benzoxazin-3-yl]-N-methylacetamide (Intermediate 13, 10.0 g, 43.7 mmol) was added portion wise over approximately 90 min and then held at 80° C. over night. Water (100 mL) was added and the mixture stirred at 40° C. The organic phase was collected and washed with aqueous sodium hydrogen carbonate (100 mL, 5.25% w/w) at 40° C. The organic phase was cooled to 10° C. and stirred over night. Isopropanol (100 mL) was added and the solid collected by filtration and dried under vacuum at 40° C. The title compound was obtained as an off-white solid (9.29 g, 22.3 mmol, 95.7% w/w, ee 98.4%, 50.9% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09394291B2
Source datasetuspto-grants-2016_07
ORD IDord-4d5f5eca125648468878a259a2a5dc42
Source noteuspto-grants-2016_07