HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 493352Generated: October 30, 2026
2-Mercaptoethanol → HCID 22036258, compound
https://huagongshe.com/reaction/493352
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2-Mercaptoethanol | HCID 1567 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Tert-butyl 4-(3-chloropyrazin-2-yl)piperazine-1-carboxylate | HCID 11150691 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | HCID 22036258 | HCID 22036258 | 65.2% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07534794B2 |
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| Source dataset | uspto-grants-2009_05 |
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| ORD ID | ord-11fdea6c19974d80a7652e17fcd16d31 |
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| Source note | uspto-grants-2009_05 |
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