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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 220556Generated: October 29, 2026

5-Methyl-1-phenyl-1H-pyrazole-4-carboxaldehyde → 3'-Chloro-4-(3-methyl-1-phenyl-1H-pyrazol-4-ylmethyl)-3,4,5,6-tetrahydro-2H-[1,2']bipyrazinyl

https://huagongshe.com/reaction/220556

Reaction equation

Participants

RoleNameHCIDCharge
Reactant5-Methyl-1-phenyl-1H-pyrazole-4-carboxaldehydeHCID 2776437—
ReactantSodium triacetoxyborohydrideHCID 5049666—
Reactant2-Chloro-3-(piperazin-1-yl)pyrazineHCID 14086438—
SolventTetrahydrofuranHCID 8028—
Product3'-Chloro-4-(3-methyl-1-phenyl-1H-pyrazol-4-ylmethyl)-3,4,5,6-tetrahydro-2H-[1,2']bipyrazinylHCID 5943822196.5%

Reaction Steps

Stir together 3′-chloro-3,4,5,6-tetrahydro-2H-[1,2′]bipyrazinyl (2.00 g, 10.07 mmol) and 5-methyl-1-phenyl-1H-pyrazole-4-carbaldehyde (2.25 g, 12.08 mmol) in dry tetrahydrofuran (10 mL) at room temperature for 10 min., under nitrogen. Add sodium triacetoxyborohydride (3.20 g, 15.10 mmol) and stir reaction for 1 hr. Quench reaction mixture with saturated aq. sodium bicarbonate (30 mL), then extract with DCM (3×20 mL) and pass through an IST Phase Separator Frit®. Concentrate and purify (silica gel chromatography, eluting with 0:100 to 5:95 methanol:DCM). Concentrate and dry in vacuum oven to give the free base as a brown oil (3.585 g, 96.5%). MS (ES): m/z=369 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08202873B2
Source datasetuspto-grants-2012_06
ORD IDord-30f3c4039885447fa9638ef4e1e44854
Source noteuspto-grants-2012_06