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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1054170Generated: October 27, 2026

Propylphosphonic anhydride → Ethyl {7-chloro-4-[(3-oxo-3,4-dihydro-2H-1,4-benzoxazin-6-yl)carbonyl]-3,4-dihydro-2H-1,4-benzoxazin-3-yl}acetate

https://huagongshe.com/reaction/1054170

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPropylphosphonic anhydrideHCID 111923—
Reactant3-Oxo-3,4-dihydro-2H-1,4-benzoxazine-6-carboxylic acidHCID 706121—
ReactantEthyl (7-chloro-3,4-dihydro-2H-1,4-benzoxazin-3-yl)acetateHCID 131736329—
SolventEthyl AcetateHCID 8857—
ProductEthyl {7-chloro-4-[(3-oxo-3,4-dihydro-2H-1,4-benzoxazin-6-yl)carbonyl]-3,4-dihydro-2H-1,4-benzoxazin-3-yl}acetateHCID 131736328101%

Reaction Conditions

Temperature160 °C

Reaction Steps

Ethyl (7-chloro-3,4-dihydro-2H-1,4-benzoxazin-3-yl)acetate (Intermediate 20, 0.67 g, 2.62 mmol), 3-oxo-3,4-dihydro-2H-1,4-benzoxazine-6-carboxylic acid (0.607 g, 3.14 mmol), and TEA (1.090 mL, 7.86 mmol) were dissolved in EtOAc (15 mL). Then T3P (50 wt. % in EtOAc, 3.12 mL, 5.24 mmol) was added and the mixture was heated in a microwave reactor for 2 h at 160° C. EtOAc (100 mL) was added and the mixture was washed with sat. aq. NaHCO3 (100 mL), 1 M HCl (100 mL) and brine (100 mL). The mixture was dried by passage through a phase separator. Concentration under reduced pressure gave 1.14 g of an oil that was purified by flash chromatography on silica gel using a gradient from 12% to 100% of EtOAc in heptane as eluent. Concentration to dryness gave the title compound (0.530 g, 46.9%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09394291B2
Source datasetuspto-grants-2016_07
ORD IDord-08bca519ba2843c3ab550c96d8563b79
Source noteuspto-grants-2016_07