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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 493352Generated: October 30, 2026

2-Mercaptoethanol → HCID 22036258, compound

https://huagongshe.com/reaction/493352

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-MercaptoethanolHCID 1567—
ReactantSodium HydroxideHCID 14798—
ReactantTert-butyl 4-(3-chloropyrazin-2-yl)piperazine-1-carboxylateHCID 11150691—
SolventWaterHCID 962—
Solvent1,4-DioxaneHCID 31275—
ProductHCID 22036258HCID 2203625865.2%

Reaction Conditions

Temperature100 °C

Reaction Steps

Sodium hydroxide (0.92 g, 23 mmol) was dissolved in water (9 mL) and dioxane (15 mL). 2-Mercaptoethanol (0.54 mL, 7.7 mmol) was added while stirring and 2-chloro-3-(4-tert-butoxycarbonyl-1-piperazinyl)pyrazine (2.3 g, 7.7 mmol, from Example 52, step 1) in dioxane (10 mL) was added. The reaction mixture was heated at 100° C. for 22 h. After cooling to room temperature, it was extracted with EtOAc. The organic layer was dried (K2CO3) and the solvent was removed under reduced pressure. The residue was purified by chromatography on silica gel using hexane/ EtOAc (1:1) as eluent to give 1.71 g (65%) of the title compound as an orange oil. MS m/z 341 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07534794B2
Source datasetuspto-grants-2009_05
ORD IDord-11fdea6c19974d80a7652e17fcd16d31
Source noteuspto-grants-2009_05