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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1440694Generated: October 30, 2026

Triethylamine → Ethyl cis-[4-(4-amino-5-chloro-2-methoxybenzamido)-3-methoxypiperidino]formate

https://huagongshe.com/reaction/1440694

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantEthyl chloroformateHCID 10928—
ReactantEthyl cis-(4-amino-3-methoxypiperidino)formateHCID 13677746—
Reactant4-Amino-3-chloro-5-methoxybenzoic acidHCID 15164586—
SolventTetrahydrofuranHCID 8028—
ProductEthyl cis-[4-(4-amino-5-chloro-2-methoxybenzamido)-3-methoxypiperidino]formateHCID 11132816—

Reaction Steps

To a mixture of 33.3 g of 4-amino-5-chloro-3-methoxybenzoic acid, 27.0 ml of triethylamine, and 450 ml of tetrahydrofuran, 16.2 ml of ethyl chloroformate was added dropwise with stirring under ice-cooling. Stirring was continued for 1.5 hours under ice-cooling, a solution of 35.0 g of ethyl cis-(4-amino-3-methoxypiperidino)formate in 50 ml of tetrahydrofuran was added dropwise. After being stirred for 20 hours at room temperature, the reaction mixture was concentrated under reduced pressure. Water was added to the residue, and the mixture was extracted with dichloromethane. The extract was washed with aqueous potassium carbonate solution, dried over anhydrous sodium sulfate, and then concentrated under reduced pressure. The residue was washed with diethyl ether to give 44.5 g of colorless crystals.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05500422
Source datasetuspto-grants-1996_03
ORD IDord-8b16be34c60b45eeb20d8cb0bdfcf621
Source noteuspto-grants-1996_03