Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1192681Generated: November 3, 2026

Tetrahydrofuran → HCID 58368419, compound

https://huagongshe.com/reaction/1192681

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
ReactantAmmonium AcetateHCID 517165—
ReactantSodium cyanoborohydrideHCID 5003444—
ReactantHCID 58368607HCID 58368607—
SolventMethanolHCID 887—
SolventAcetonitrileHCID 6342—
ProductHCID 58368419HCID 58368419—

Reaction Conditions

Temperature65 °C

Reaction Steps

A mixture of 1-{5-chloro-8-[4-(pyrazin-2-ylcarbonyl)piperazin-1-yl]quinolin-7-yl}ethanone (0.028 g, 0.071 mmol) and ammonium acetate (0.0545 g, 0.707 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, to the resulting mixture was added 1.0 M sodium cyanoborohydride in tetrahydrofuran (0.17 mL, 0.17 mmol). The reaction was heated at 65° C. overnight. The mixture was cooled to room temperature, quenched with sat. NaHCO3 solution, extracted with dichloromethane, dried over MgSO4 and concentrated to give the desired product. LCMS calculated for C20H22ClN6O (M+H)+: m/z=397.2; Found: 397.1.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08680108B2
Source datasetuspto-grants-2014_03
ORD IDord-29cb9d0229534effa241ce56fcdf554f
Source noteuspto-grants-2014_03