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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1877963Generated: November 2, 2026

6-[5-(3-Chloropropyl)imidazol-1-ylmethyl]biphenyl-3-carbonitrile → HCID 69438002, compound

https://huagongshe.com/reaction/1877963

Reaction equation

Participants

RoleNameHCIDCharge
Reactant6-[5-(3-Chloropropyl)imidazol-1-ylmethyl]biphenyl-3-carbonitrileHCID 58827070—
ReactantKOtBu THFHCID 66863523—
SolventTetrahydrofuranHCID 8028—
ProductHCID 69438002HCID 69438002—

Reaction Steps

To a solution of 6-[5-(3-chloropropyl)imidazol-1-ylmethyl]biphenyl-3-carbonitrile (1.0 g, 3.0 mmol) in THF (16 mL) at 0° C. is added t-BuOK/THF (1.0 M, 6 mL, 6.0 mmol). The mixture is warmed up to ambient temperature and stirred for 2 h. The reaction mixture is quenched by saturated aqueous NH4Cl and partitioned between CH2Cl2 and brine. The organic layer is washed by brine, dried over anhydrous Na2SO4 and concentrated to give the crude oil, which is subjected to flash chromatography (silica gel) eluting with MeOH:CH2Cl2 to yield the desired compound. MS (ESI) m/z 300 (M+H); 1H NMR (400 MHz, CDCl3) δ ppm 1.50-1.66 (m, 1 H), 1.73-1.83 (m, 1 H), 1.83-1.95 (m, 1 H), 1.95-2.16 (m, 1 H), 2.68-2.95 (m, 2 H), 5.28 (dd, J=8.5, 5.2 Hz, 1 H), 6.83 (s, 1 H), 7.01-7.15 (m, 2 H), 7.27-7.35 (m, 2 H), 7.43-7.54 (m, 3 H), 7.58 (s, 1 H), 7.62 (d, J=8.3 Hz, 1 H). Resolution of the enantiomers of the title compound is achieved by Chiral HPLC using the ChiralPak AD column with a 20% IPA/Hexane mobile phase.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08314097B2
Source datasetuspto-grants-2012_11
ORD IDord-93047093a9b548cfb1d55e39d1bfe06b
Source noteuspto-grants-2012_11