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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1264657Generated: October 27, 2026

Triethylamine → (trans)-Ethyl 4-[[[(7-chloro-2,3-dihydro-1,4-benzodioxin-5-yl)carbonyl]-amino]methyl]-3-ethoxy-1-piperidinecarboxylate

https://huagongshe.com/reaction/1264657

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantEthyl chloroformateHCID 10928—
Reactant7-Chloro-2,3-dihydro-1,4-benzodioxine-5-carboxylic acidHCID 18613662—
ReactantEthyl (trans)-4-(aminomethyl)-3-ethoxy-1-piperidinecarboxylateHCID 86589667—
SolventChloroformHCID 6212—
Product(trans)-Ethyl 4-[[[(7-chloro-2,3-dihydro-1,4-benzodioxin-5-yl)carbonyl]-amino]methyl]-3-ethoxy-1-piperidinecarboxylateHCID 13172384593.7%

Reaction Steps

At a temperature below 10° C., triethylamine (0.01 mol) was added to 7-chloro-2,3-dihydro-1,4-benzodioxin-5-carboxylic acid (0.01 mol) in chloroform (40 ml). Ethyl chloroformate 01 mol) was added at a temperature below 10IC and the mixture was stirred for 30 minutes at a temperature below 10° C. This mixture was added to a solution of intermediate (14) (0.01 mol) in chloroform (20 ml), at a temperature below 10° C. The reaction mixture was stirred for 30 minutes then washed with a 5% HCl solution, with water, dried, filtered and the solvent was evaporated, yielding 4 g of (trans)-ethyl 4-[[[(7-chloro-2,3-dihydro-1,4-benzodioxin-5-yl)carbonyl]-amino]methyl]-3-ethoxy-1-piperidinecarboxylate (intermediate 15).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06544997B1
Source datasetuspto-grants-2003_04
ORD IDord-9c0ebb7c8bd244aba26639c53ea16ce0
Source noteuspto-grants-2003_04