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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1466117Generated: October 27, 2026

Sodium cyanoborohydride → 6-(4-(4-Nitrophenethyl)-3-oxopiperazin-1-yl)-5,6,7,8-tetrahydronaphthalene-2-carbonitrile

https://huagongshe.com/reaction/1466117

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium cyanoborohydrideHCID 5003444—
Reactant6-Oxo-5,6,7,8-tetrahydronaphthalene-2-carbonitrileHCID 16244504—
Reactant1-[2-(4-Nitrophenyl)ethyl]piperazin-2-oneHCID 89524891—
CatalystTitanium isopropoxideHCID 11026—
SolventEthanolHCID 702—
SolventEthyl AcetateHCID 8857—
Product6-(4-(4-Nitrophenethyl)-3-oxopiperazin-1-yl)-5,6,7,8-tetrahydronaphthalene-2-carbonitrileHCID 71525685—

Reaction Steps

A mixture of 6-Oxo-5,6,7,8-tetrahydronaphthalene-2-carbonitrile (24 mg, 0.14 mmol) and 1-[2-(4-nitrophenyl)ethyl]piperazin-2-one (20 mg, 0.070 mmol) was treated with titanium(IV) isopropoxide (0.10 ml, 0.35 mmol) for 30 minutes. Then the reaction was diluted with ethanol (5 mL), and sodium cyanoborohydride (44 mg, 0.70 mmol) was added. The reaction was stirred at RT overnight. The reaction was diluted with EtOAc, washed with brine, dried over sodium sulfate, and concentrated to give the crude residue. The desired product was purified by reverse phase HPLC (AcCN-Water with 0.1% TFA). LC-MS (IE, m/z): 405 [M+1]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08999990B2
Source datasetuspto-grants-2015_04
ORD IDord-ca3a5800606842b7a85fa0f0b6009b19
Source noteuspto-grants-2015_04