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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1396653Generated: November 2, 2026

Oxane-4-carboxylic acid → HCID 58575079, compound

https://huagongshe.com/reaction/1396653

Reaction equation

Participants

RoleNameHCIDCharge
ReactantOxane-4-carboxylic acidHCID 219302—
ReactantSodium BicarbonateHCID 516892—
ReactantPyBroPHCID 2733179—
ReactantMethyl 3-chloro-2-hydrazino7-methylquinoxaline-6-carboxylateHCID 86660662—
SolventChloroformHCID 6212—
SolventDichloromethaneHCID 6344—
SolventTriethylamineHCID 8471—
ProductHCID 58575079HCID 5857507964.1%

Reaction Steps

To a mixture of 10 g of methyl 3-chloro-2-hydrazino-7-methylquinoxaline-6-carboxylate, 5.9 g of tetrahydro-2H-pyran-4-carboxylic acid, 16 mL of triethylamine, and 100 mL of dichloromethane was added 21 g of bromo(tripyrrolidin-1-yl)phosphonium hexafluorophosphate, followed by stirring at room temperature for 9 hours. To the reaction mixture were added saturated aqueous sodium hydrogen carbonate solution and chloroform. The solid was collected by filtration and washed with ethyl acetate to obtain 9.1 g of methyl 3-chloro-7-methyl-2-[2-(tetrahydro-2H-pyran-4-ylcarbonyl)hydrazino]quinoxaline-6-carboxylate as a pink solid. Further, to the filtrate obtained above was added chloroform, and then the aqueous layer was separated. The organic layer was washed with saturated brine and dried over anhydrous magnesium sulfate. The solvent was evaporated under reduced pressure and the obtained residue was washed with ethyl acetate to obtain 3.58 g of methyl 3-chloro-7-methyl-2-[2-(tetrahydro-2H-pyran-4-ylcarbonyl)hydrazino]quinoxaline-6-carboxylate as a colorless solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08901126B2
Source datasetuspto-grants-2014_12
ORD IDord-36d5283fa38146f480eaf0fe33df2a02
Source noteuspto-grants-2014_12