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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 129387Generated: October 30, 2026

Water → HCID 15278639, compound

https://huagongshe.com/reaction/129387

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantTriethylamineHCID 8471—
ReactantHCID 15278638HCID 15278638—
ReactantMethyl 2-carbamoylcyclohex-1-ene-1-carboxylateHCID 15334633—
SolventBenzeneHCID 241—
ProductHCID 15278639HCID 15278639—

Reaction Steps

First, 0.44 g of N-(7-fluoro-4-propargyl-2H-1,4-benzoxazine-3(4H)-one-6-yl)-acetimidoylchloride and 0.29 g of 3,4,5,6-tetrahydrophthalamic acid monomethyl ester were dissolved in 15 ml of benzene, and 0.17 g of triethylamine was added to the solution at room temperature. After that the stirring was continued for 2 hr at 60° C. After letting the reaction liquid stand to cool the same, it was poured into cool water, and then the organic layer was separated therefrom. The organic layer was washed first with water and then with saturated brine, and then dried by using anhydrous magnesium sulfate. The solvent was concentrated, and then the residue was treated by silica gel column chromatography (development solvent: ethyl acetate/n-hexane) to obtain N-acetyl-N-(7-fluoro-4-propargyl-2H-1,4-benzoxazine-3(4H)-one-6-yl)-3,4,5,6tetrahydrophthalamic acid methyl ester. The melting point was 153°-154° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05468719
Source datasetuspto-grants-1995_11
ORD IDord-a5cfd52a4985444cae2a1db220ee2bdd
Source noteuspto-grants-1995_11