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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1381820Generated: October 26, 2026

1(2H)-Pyridazinecarboxylic acid, tetrahydro-, ethyl ester → 2-[7-fluoro-2H-1,4-benzoxazin-3(4H)-on-6-yl]-hexahydro-1H-(1,2,4)-triazolo (1,2-a) pyridazine-1,3-dione

https://huagongshe.com/reaction/1381820

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1(2H)-Pyridazinecarboxylic acid, tetrahydro-, ethyl esterHCID 3014377—
Reactant6-isocyanato-7-fluoro-2H-1,4-benzoxazin-3(4H)-oneHCID 14402873—
CatalystTriethylamineHCID 8471—
Solvent1,4-DioxaneHCID 31275—
Product2-[7-fluoro-2H-1,4-benzoxazin-3(4H)-on-6-yl]-hexahydro-1H-(1,2,4)-triazolo (1,2-a) pyridazine-1,3-dioneHCID 1440287474.7%

Reaction Steps

A mixture composed of 6-isocyanato-7-fluoro-2H-1,4-benzoxazin-3(4H)-one (2.14 g), 1-ethoxycarbonylhexahydropyridazine (1.62 g) and dioxane (30 ml) is treated with a few drops of triethylamine, stirred at an ambient temperature for 2 hours, and left overnight. The reaction mixture is made free from dioxane by evaporation in vacuo, mixed with methanol (30 ml) containing a catalytic amount of sodium, and refluxed for 2 hours. After removal of methanol by evaporation in vacuo, the resultant solid is collected, and washed with water to obtain an end product 2-[7-fluoro-2H-1,4-benzoxazin-3(4H)-on-6-yl]-hexahydro-1H-(1,2,4)-triazolo (1,2-a) pyridazine-1,3-dione (2.45 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04804394
Source datasetuspto-grants-1989_02
ORD IDord-40b3fb53dace4500809f03c4b7c06459
Source noteuspto-grants-1989_02