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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 220507Generated: October 26, 2026

1,2-Dichloroethane → HCID 68595010, compound

https://huagongshe.com/reaction/220507

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,2-DichloroethaneHCID 11—
ReactantSodium triacetoxyborohydrideHCID 5049666—
Reactant1-(2-hydroxyethyl)-1H-pyrazole-4-carbaldehydeHCID 24702608—
Reactant2-(4-Fluorophenyl)-3-(piperazin-1-yl)pyrazineHCID 67366959—
ProductHCID 68595010HCID 6859501062%

Reaction Steps

Dissolve 3′-(4-fluoro-phenyl)-3,4,5,6-tetrahydro-2H-[1,2′]bipyrazinyl (0.320 g, 1.24 mmol) in DCE (5 mL). Add 1-(2-hydroxy-ethyl)-1H-pyrazole-4-carbaldehyde (0.243 g, 1.73 mmol), and stir at room temperature. Add sodium triacetoxyborohydride (0.394 g, 1.86 mmol) and stir at room temperature for 18 hr. Purify via SCX chromatography, followed by silica gel chromatography, eluting with 20:80 then 0:100 hexanes:ethyl acetate then 5:95 methanol:ethyl acetate then 10:90 methanol:ethyl acetate, to give the free base of the title compound (296 mg, 62%). Dissolve the free base (0.290 g, 0.760 mmol) in acetonitrile and add 1N aqueous HCl solution (913 μL, 0.913 mmol) and shake at ambient temperature for 30 min. Freeze and lyophilize to give the title compound (315 mg, 99%). MS (ES): m/z=383 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08202873B2
Source datasetuspto-grants-2012_06
ORD IDord-a4ea4eaacb9c452998c1557e13a5150f
Source noteuspto-grants-2012_06