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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1192568Generated: November 1, 2026

Tetrahydrofuran → HCID 58368524, compound

https://huagongshe.com/reaction/1192568

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
ReactantAmmonium AcetateHCID 517165—
ReactantSodium cyanoborohydrideHCID 5003444—
ReactantHCID 58368595HCID 58368595—
SolventMethanolHCID 887—
SolventAcetonitrileHCID 6342—
ProductHCID 58368524HCID 58368524—

Reaction Conditions

Temperature65 °C

Reaction Steps

A mixture of 1-[5-ethyl-8-(3-fluorophenyl)quinolin-7-yl]ethanone (6.1 mg, 0.021 mmol) and ammonium acetate (0.017 g, 0.22 mmol) in methanol (0.3 mL) and acetonitrile (0.3 mL) was heated at 65° C. in a sealed tube for 1 hour. After cooling to room temperature, 1.0 M sodium cyanoborohydride in tetrahydrofuran (0.052 mL, 0.052 mmol) was added to the mixture. The reaction was heated at 65° C. overnight. The mixture was cooled to room temperature, quenched with sat. NaHCO3 solution and extracted with dichloromethane. The combined organic layers were dried over MgSO4 and concentrated to give the desired product. LCMS calculated for C19H20FN2 (M+H)+: m/z=295.2; Found: 295.1.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08680108B2
Source datasetuspto-grants-2014_03
ORD IDord-5b4cd867a0bc44d6b2389ded2e8a23ef
Source noteuspto-grants-2014_03