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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1386783Generated: October 31, 2026

Ethyl chloroformate → 1-Ethoxycarbonyl-4-((benzothiazol-2-yl)methyl)piperidine

https://huagongshe.com/reaction/1386783

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl chloroformateHCID 10928—
Reactant1-Benzyl-4-((benzothiazol-2-yl)methyl)piperidineHCID 21180710—
SolventTetrahydrofuranHCID 8028—
Product1-Ethoxycarbonyl-4-((benzothiazol-2-yl)methyl)piperidineHCID 2118077967.8%

Reaction Steps

A solution of 500 mg of 1-benzyl-4-((benzothiazol-2-yl)methyl)piperidine (from EXAMPLE 163, Step D) in 10 mL of THF was added 185 mg of ethyl chloroformate at rt. The reaction was stirred at rt for 5 h. The reaction mixture was partitioned between H2O and EtOAc. The aqueous phase was extracted with EtOAc (3×). The combined organic phases were washed with sat'd NaCl and dried over MgSO4. Concentration afforded 320 mg of the title compound as a oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06265434B1
Source datasetuspto-grants-2001_07
ORD IDord-d1675590bc0d469b85cf20ad9de1a05f
Source noteuspto-grants-2001_07