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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2303925Generated: November 3, 2026

Water → HCID 86586145, compound

https://huagongshe.com/reaction/2303925

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactant1-Bromo-3-chloropropaneHCID 8006—
ReactantSodium hydrideHCID 24758—
ReactantHCID 14950891HCID 14950891—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
ProductHCID 86586145HCID 86586145—

Reaction Steps

To a solution of 5H-dibenzo[a,d]cycloheptene-5-carbonitrile (described in J. Med Chem. 1994, 37, 804-810) (500 mg) in DMF (10 ml) were added 60% sodium hydride (110 mg) and 1-bromo-3- chloropropane (0.30 ml) and the mixture was stirred at room temperature for 1 hours. Water and ethyl acetate were added to the reaction mixture, the organic layer was separated and washed with saturated aqueous sodium chloride, and dried over magnesium sulfate. The solvent was distilled off under reduced pressure to give 5-(3-chloropropyl-5H-dibenzo[a,d]cycloheptene-5-carbonitrile. Without purification, to a solution obtained chloride in DMF (10 ml) were added 4-(4-chlorophenyl)-4-hydroxypiperidine (650 mg), potassium carbonate (950 mg), and potassium iodide (50 mg) and the mixture was stirred at 70° C. for 24 hours. Water and ethyl acetate were added to the reaction mixture, the organic layer was separated and washed with saturated aqueous sodium chloride, and dried over magnesium sulfate. The solvent was distilled off under reduced pressure. The residue was purified by silica gel chromatography eluting with ethyl acetate-hexane (1:1) to give the titled compound (700 mg). 1H-NMR (CDCl3) d: 1.22-1.34(2H,m), 1.60-1.80(3H,m), 1.93-1.99(2H,m), 2.16-2.28(6H,m), 2.56-2.60(2H,m), 6.98(2H,s), 7.25-7.47(10H,m), 8.00-8.03(2H,m). MS m/z: 469(M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06433165B1
Source datasetuspto-grants-2002_08
ORD IDord-b9f41b077fbd42e2b64584e0fefbc962
Source noteuspto-grants-2002_08