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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 883277Generated: October 29, 2026

1-Phenylpiperazine → HCID 25064641, compound

https://huagongshe.com/reaction/883277

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 Å 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 numberUS08236806B2
Source datasetuspto-grants-2012_08
ORD IDord-b1b476a0cace40ab9c3df65deceb3e88
Source noteuspto-grants-2012_08