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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1432022Generated: October 30, 2026

Methanol → 4-((R)-1-(4-(((R)-1-(3 4-dichlorobenzenesulfonyl)-3-oxo-1,2,3,4-tetra-hydropyrazin-2-yl)methyl)-1H-1,2,3-triazol-1-yl)ethyl)benzaldehyde

https://huagongshe.com/reaction/1432022

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
Reactant(R)-4-(3,4-Dichlorobenzenesulfonyl)-3-((1-((R)-1-(4-(hydroxymethyl)-phenyl)ethyl)-1H-1,2,3-triazol-4-yl)methyl)-3,4-dihydropyrazin-2(1H)-oneHCID 57932459—
CatalystManganese dioxideHCID 14801—
SolventDichloromethaneHCID 6344—
Product4-((R)-1-(4-(((R)-1-(3 4-dichlorobenzenesulfonyl)-3-oxo-1,2,3,4-tetra-hydropyrazin-2-yl)methyl)-1H-1,2,3-triazol-1-yl)ethyl)benzaldehydeHCID 57932452—

Reaction Steps

To a solution of (R)-4-(3,4-dichlorobenzenesulfonyl)-3-((1-((R)-1-(4-(hydroxymethyl)-phenyl)ethyl)-1H-1,2,3-triazol-4-yl)methyl)-3,4-dihydropyrazin-2(1H)-one (0.461 g, 0.882 mmol) in CH2Cl2 (100 mL) was added MnO2 (1.92 g, 22.1 mmol). After 1.5 h, MeOH (20 mL) was added. After the reaction mixture had stirred for 15 min, it was filtered through Celite and the solid was washed with CH2Cl2/MeOH (10/1). The solvent was removed under reduced pressure and dried in vacuo to yield the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07612060B2
Source datasetuspto-grants-2009_11
ORD IDord-21d8013b59324b2c9d9c71b5c0f48c0c
Source noteuspto-grants-2009_11