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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 220510Generated: October 26, 2026

1,2-Dichloroethane → 2-{4-[3'-(2-Fluoro-phenyl)-2,3,5,6-tetrahydro-[1,2']bipyrazinyl-4-ylmethyl]-pyrazol-1-yl}-ethanol hydrochloride

https://huagongshe.com/reaction/220510

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,2-DichloroethaneHCID 11—
ReactantSodium triacetoxyborohydrideHCID 5049666—
Reactant1-(2-hydroxyethyl)-1H-pyrazole-4-carbaldehydeHCID 24702608—
Reactant3'-(2-Fluoro-phenyl)-3,4,5,6-tetrahydro-2h-[1,2']bipyrazinylHCID 67367520—
Product2-{4-[3'-(2-Fluoro-phenyl)-2,3,5,6-tetrahydro-[1,2']bipyrazinyl-4-ylmethyl]-pyrazol-1-yl}-ethanol hydrochlorideHCID 6859424937%

Reaction Steps

Dissolve 3′-(2-fluoro-phenyl)-3,4,5,6-tetrahydro-2H-[1,2′]bipyrazinyl (0.213 g, 0.825 mmol) in DCE (5 mL). Add 1-(2-hydroxy-ethyl)-1H-pyrazole-4-carbaldehyde (0.137 g, 0.990 mmol) followed by sodium triacetoxyborohydride (0.262 g, 1.24 mmol) and stir at ambient temperature for 18 hr. Add additional 1-(2-hydroxy-ethyl)-1H-pyrazole-4-carbaldehyde (0.093 g, 0.663 mmol) and stir at ambient temperature for 18 hr. Purify via SCX chromatography followed by silica gel chromatography, (eluting with 100:0 to 0:100 hexanes:ethyl acetate, then 10:90 methanol:ethyl acetate), to give the free base of the title compound (116 mg, 37%). Dissolve the free base (0.114 g, 0.298 mmol) in methanol and add a solution of ammonium chloride (0.016 g, 0.298 mmol) in a minimal volume of methanol. Shake for 18 hr. at ambient temperature and concentrate to give the title compound (125 mg, 100%). MS (ES): m/z=383[M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08202873B2
Source datasetuspto-grants-2012_06
ORD IDord-2573102a1a6441df97adadc0dfd7b9b3
Source noteuspto-grants-2012_06