Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 220524Generated: October 31, 2026

Hydrochloric Acid → 4-(1-Ethyl-3,5-dimethyl-1H-pyrazol-4-ylmethyl)-3'-(4-fluoro-phenyl)-3,4,5,6-tetrahydro-2H-[1,2']bipyrazinyl hydrochloride

https://huagongshe.com/reaction/220524

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantSodium HydroxideHCID 14798—
Reactant1-Ethyl-3,5-dimethyl-1H-pyrazole-4-carbaldehydeHCID 3157461—
ReactantSodium triacetoxyborohydrideHCID 5049666—
Reactant3'-(4-fluoro-phenyl)-3,4,5,6-tetrahydro-2H-[1,2']bipyrazinyl dihydrochlorideHCID 67366958—
SolventAcetonitrileHCID 6342—
SolventDichloromethaneHCID 6344—
SolventTetrahydrofuranHCID 8028—
Product4-(1-Ethyl-3,5-dimethyl-1H-pyrazol-4-ylmethyl)-3'-(4-fluoro-phenyl)-3,4,5,6-tetrahydro-2H-[1,2']bipyrazinyl hydrochlorideHCID 6859695015%

Reaction Steps

To a stirred suspension of 3′-(4-fluoro-phenyl)-3,4,5,6-tetrahydro-2H-[1,2′]bipyrazinyl dihydrochloride (0.3 g, 0.906 mmol, 1 eq) and 1-ethyl-3,5-dimethyl-1H-pyrazole-4-carbaldehyde (207 mg, 1.36 mmol, 1.5 eq) in tetrahydrofuran (10 mL) add sodium triacetoxyborohydride (480 mg, 2.26 mmol, 2.5 eq) in one portion as a solid. Stir the mixture at room temperature under nitrogen for 19 hr. Add 2M aqueous sodium hydroxide solution (10 ml) and DCM (20 ml) separate and extract the aqueous layer with DCM (20 ml). Combine the organics, dry over magnesium sulfate, filter and concentrate. Purify by high pH reverse phase HPLC. Dissolve this material (49 mg, 0.12 mmol), in the minimum quantity of 50% aqueous acetonitrile. Add 2M aqueous hydrogen chloride (60 μL, 0.12 mmol) and lyophilize to give the title compound (58 mg, 15%). MS (ES): m/z=395.2 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08202873B2
Source datasetuspto-grants-2012_06
ORD IDord-b8e8b01beb84434e9f3da647114b4aad
Source noteuspto-grants-2012_06