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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1780640Generated: October 30, 2026

Water → HCID 13731306, compound

https://huagongshe.com/reaction/1780640

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantPropargyl bromideHCID 7842—
ReactantSodium hydrideHCID 24758—
ReactantHCID 15839682HCID 15839682—
SolventDimethylformamideHCID 6228—
ProductHCID 13731306HCID 1373130640.8%

Reaction Steps

While kept under N2, 0.30 g (7.4 mmol) of sodium hydride (60% dispersion in oil) was washed with 1 ml pentanes and then suspended in 2 ml anhydrous dimethylformamide. A solution of 1.36 g (6.9 mmol) of 6-amino-7-fluoro-2-methyl-2H-1,4-benzoxazin-3(4H)-one in 10 ml of dimethylformamide was added to the sodium hydride slurry slowly by syringe with ice cooling and the reaction mixture was stirred at room temperature for 0.5 hr. There was then added 0.77 ml (8.6 mmol) of propargyl bromide by syringe with ice bath cooling. The reaction mixture was allowed to warm to room temperature, stirred for 84 hours and then poured into 50 ml of water. The resulting mixture was extracted with EtOAc (2×50 ml) and the organic layers were combined and washed with water (3×50 ml), dried over MgSO4 and filtered. The solvent was removed in vacuo to yield a golden solid which was recrystallized from chloroform to yield 0.66 g of 6-amino-7-fluoro-2-methyl-4-propargyl-2H-1,4-benzoxazin-3(4H)-one as a brown solid, m.p. 142°-145° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05631209
Source datasetuspto-grants-1997_05
ORD IDord-0033a6a9fd3940968bd7e0009805da43
Source noteuspto-grants-1997_05