Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2182130Generated: November 3, 2026

Potassium Hydroxide → Tert-butyl 4-(6-((3-chlorobenzyl)oxy)pyrazin-2-yl)piperazine-1-carboxylate

https://huagongshe.com/reaction/2182130

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium HydroxideHCID 14797—
Reactant3-Chlorobenzyl alcoholHCID 70117—
ReactantTert-butyl 4-(6-chloropyrazin-2-YL)piperazine-1-carboxylateHCID 18186946—
Catalyst18-Crown-6HCID 28557—
SolventTolueneHCID 1140—
ProductTert-butyl 4-(6-((3-chlorobenzyl)oxy)pyrazin-2-yl)piperazine-1-carboxylateHCID 6973279893.9%

Reaction Steps

A mixture of 6′-chloro-2,3,5,6-tetrahydro-[1,2′]bipyrazinyl-4-carboxylic acid tert-butyl ester (I-1a) (300 mg, 1.0 mmol), 3-chlorobenzyl alcohol (0.142 mL, 1.2 mmol), KOH (191 mg, 3.4 mmol) and 18-crown-6 (10.6 mg, 0.04 mmol) in toluene (6 mL) was stirred at reflux for 5.5 h and concentrated in vacuo. The residue was partitioned between H2O (30 mL) and CH2Cl2 (30 mL). The aqueous phase was separated and extracted with CH2Cl2 (2×30 mL). The combined organic extracts were dried and concentrated in vacuo. The crude product was purified by preparative TLC (5% MeOH in CH2Cl2) to afford the title compound (I-1b) (380 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06894050B2
Source datasetuspto-grants-2005_05
ORD IDord-90dea26b23da42a99810b7f060c9deb5
Source noteuspto-grants-2005_05