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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1789763Generated: November 1, 2026

2-Mercaptoethanol → HCID 22036258, compound

https://huagongshe.com/reaction/1789763

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 numberUS07071180B2
Source datasetuspto-grants-2006_07
ORD IDord-ce211c22d47645f9b378ccf64f84926e
Source noteuspto-grants-2006_07