Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 220515Generated: October 30, 2026

1,2-Dichloroethane → 4-(1-Ethyl-5-methyl-1h-pyrazol-4-ylmethyl)-3'-(4-fluoro-phenyl)-3,4,5,6-tetrahydro-2h-[1,2']bipyrazine hydrochloride

https://huagongshe.com/reaction/220515

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,2-DichloroethaneHCID 11—
Reactant1-Ethyl-5-methyl-1H-pyrazole-4-carbaldehydeHCID 573204—
ReactantSodium triacetoxyborohydrideHCID 5049666—
Reactant2-(4-Fluorophenyl)-3-(piperazin-1-yl)pyrazineHCID 67366959—
Product4-(1-Ethyl-5-methyl-1h-pyrazol-4-ylmethyl)-3'-(4-fluoro-phenyl)-3,4,5,6-tetrahydro-2h-[1,2']bipyrazine hydrochlorideHCID 6859478255%

Reaction Steps

Dissolve 3′-(4-Fluoro-phenyl)-3,4,5,6-tetrahydro-2H-[1,2′]bipyrazinyl (0.183 g, 0.708 mmol) in DCE (8.5 mL). Add 1-ethyl-5-methyl-1H-pyrazole-4-carbaldehyde (0.117 g, 0.850 mmol) followed by sodium triacetoxyborohydride (0.225 g, 1.06 mmol) and stir at room temperature for 18 hr. Purify via SCX chromatography, followed by silica gel chromatography (eluting with 50:50 then 0:100 hexanes:ethyl acetate then 10:90 methanol:ethyl acetate), followed by reverse phase chromatography to give the free base of the title compound (149 mg, 55%). Dissolve the free base (0.138 g, 0.363 mmol) in methanol and add a solution of ammonium chloride (0.019 g, 0.363 mmol) in a minimal volume of methanol. Shake for 18 hr. at ambient temperature and concentrate to give 4-(1-Ethyl-5-methyl-1H-pyrazol-4-ylmethyl)-3′-(4-fluoro-phenyl)-3,4,5,6-tetrahydro-2H-[1,2′]bipyrazinyl hydrochloride (149 mg, 99%). MS (ES): m/z=381 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08202873B2
Source datasetuspto-grants-2012_06
ORD IDord-54569aaac5b94fe7b77b57ff927313d2
Source noteuspto-grants-2012_06