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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 329726Generated: November 2, 2026

Ethyl chloroformate → HCID 19871144, compound

https://huagongshe.com/reaction/329726

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl chloroformateHCID 10928—
Reactant3-AminoquinuclidineHCID 123238—
ReactantSodium BicarbonateHCID 516892—
ReactantHCID 14802116HCID 14802116—
SolventTetrahydrofuranHCID 8028—
SolventTriethylamineHCID 8471—
SolventEthyl AcetateHCID 8857—
ProductHCID 19871144HCID 19871144—

Reaction Steps

A solution of 4.2 g of 6-chloro-4-ethyl-3,4-dihydro-2-methyl-3-oxo-2H-1,4-benzoxazine-8-carboxylic acid in 100 ml of tetrahydrofuran is cooled to below 0° C. and 5 ml of triethylamine is added under stirring thereto. Further, 2.0 g of ethyl chlorocarbonate is added and the mixture is stirred for 30 minutes. To the resultant mixture is added 3.0 g of 3-aminoquinuclidine and the mixture stirred for 5 hours. After completion of the reaction, aqueous sodium hydrogen carbonate and ethyl acetate are added. The organic layer is separated, washed with water and dried over magnesium sulfate. The solvent is distilled off and the residue is converted into the corresponding hydrochloride by treating with ethanolic hydrochloric acid followed by recrystallizing from ethanol-ethyl acetate to give 6-chloro-4-ethyl-3,4-dihydro-2-methyl-3-oxo-N-(3-quinuclidinyl)-2H-1,4-benzoxazine-8-carboxamide hydrochloride, melting at 249°-252° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04892872
Source datasetuspto-grants-1990_01
ORD IDord-6098f3a0a69d4231815c95412b6d173f
Source noteuspto-grants-1990_01