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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 386990Generated: October 27, 2026

1-Phenylpiperazine → HCID 25064641, compound

https://huagongshe.com/reaction/386990

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-PhenylpiperazineHCID 7096—
ReactantDiisopropylethylamineHCID 81531—
ReactantSodium triacetoxyborohydrideHCID 5049666—
Reactant3-(1-tert-butyl-5-phenyl-1H-pyrazol-3-yl)propanalHCID 86639916—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
SolventHexaneHCID 8058—
SolventEthyl AcetateHCID 8857—
ProductHCID 25064641HCID 25064641—

Reaction Steps

3-(1-tert-butyl-5-phenyl-1H-pyrazol-3-yl)propanal (80 mg, 312 mmol) and 1-phenylpiperazine (0.047 mL, 0.312 mmol) were dissolved in 5 mL of CH2Cl2, and then 0.7 g of 4 molecular sieve powder was added thereto and stirred. Diisopropylethylamine (DIPEA; 54 mL, 0.312 mmol) was slowly added thereto, and stirred for 30 min at room temperature. Then, NaBH(OAc)3 (231 mg, 1.092 mmol) was added thereto and stirred for 12 hours at room temperature. The reaction progress and completion were confirmed by TLC. Upon completion of the reaction, water (0.1 mL) was added to the reaction mixture and then stirred for 3 min. 81 mg (64%) of target compound was obtained via column chromatography (EtOAc:Hexane=4:1, v/v).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08372844B2
Source datasetuspto-grants-2013_02
ORD IDord-05039d42d05242a8b9e2daabd24721ad
Source noteuspto-grants-2013_02