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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1504344Generated: October 31, 2026

2-Methyltetrahydrofuran → HCID 178461449, compound

https://huagongshe.com/reaction/1504344

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-MethyltetrahydrofuranHCID 7301—
ReactantSodium BicarbonateHCID 516892—
ReactantHCID 89541653HCID 89541653—
ReactantHCID 178461444HCID 178461444—
CatalystBis(di-tert-butyl(4-dimethylaminophenyl)phosphine)dichloropalladium(II)HCID 11714597—
SolventWaterHCID 962—
SolventEthyl AcetateHCID 8857—
ProductHCID 178461449HCID 17846144993%

Reaction Conditions

Temperature70 °C

Reaction Steps

To a round bottom flask was added (2S,4S)-tert-butyl 2-(4-(4-bromophenyl)-1H-imidazol-2-yl)-4-methylpyrrolidine-1-carboxylate (10 g, 24.61 mmol), (R)-(5-chloro-4-(6-(2-methyl-4-pivaloylpiperazin-1-yl)nicotinamido)-2-(trifluoromethoxy)phenyl)boronic acid (14.16 g, 26.1 mmol), sodium bicarbonate (7.24 g, 86 mmol), bis(di-tert-butyl(4-dimethylaminophenyl)phosphine)dichloropalladium(II) (0.17 g, 0.246 mmol), 2 methyltetrahydrofuran (120 mL) and water (44.3 mL) to give a suspension. The reaction mixture was degassed with nitrogen for 10 min then heated at 70° C. overnight. Water (60 mL) was added and the layers were separated. The organic layer was washed with brine, dried over Na2SO4, and evaporated to give crude product (27.3 g). The crude product was purified by flash chromatography (300 g silica gel, 20-100% EtOAc (50 min), then 100% EtOAc (20 min)) to give the title intermediate (18.8 g; 93% yield) HPLC Method B: Retention time 14.99 min.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09212168B2
Source datasetuspto-grants-2015_12
ORD IDord-d7b396af3a1e4a89bb7a53339b9d8bb1
Source noteuspto-grants-2015_12