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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1794098Generated: November 1, 2026

Pyridine → (RS) 1-Chlorocarbonyl-2-ethyl-4-tert-butoxycarbonylpiperazine

https://huagongshe.com/reaction/1794098

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantTriphosgeneHCID 94429—
Reactanttert-Butyl 3-ethylpiperazine-1-carboxylateHCID 22219867—
SolventDichloromethaneHCID 6344—
Product(RS) 1-Chlorocarbonyl-2-ethyl-4-tert-butoxycarbonylpiperazineHCID 22219864190.4%

Reaction Steps

a solution of (RS) 4-tert-butoxycarbonyl-2-ethylpiperazine (3.95 g) and pyridine (1.64 ml) in DCM (35 ml) was added dropwise to a stirred solution of triphosgene (2.1 g) in DCM (100 ml) at 0° C. under Ar. The mixture was warmed to room temperature, stirred for 30 min then washed with water (100 ml) and brine (100 ml). The organic solution was dried (sodium sulfate) and concentrated in vacuo. The residue was dissolved in isohexane, filtered and concentrated in vacuo to give the product as a clear oil (3.73 g) which was used without further purification; δH (400 MHz, CDCl3) 4.39–3.80 (4H, m), 3.39–2.69 (3H, m), 1.66 (2H, m), 1.47 (9H, s), 0.96 (2.7H, d, J 7 Hz) and 0.89 (0.3H, d, J 7 Hz); GC (150° C.-10 min-320° C.) 83%, 8.72 min.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07022707B2
Source datasetuspto-grants-2006_04
ORD IDord-c2eb39bfec434d678e055f71dfdf78c8
Source noteuspto-grants-2006_04