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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1027708Generated: October 25, 2026

2-Methyltetrahydrofuran → Pf-04937319

https://huagongshe.com/reaction/1027708

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-MethyltetrahydrofuranHCID 7301—
ReactantChlorodimethylaluminumHCID 79147—
Reactant5-Methylpyrazin-2-amineHCID 313215—
ReactantEthyl 4-(2-(dimethylcarbamoyl)pyrimidin-5-yloxy)-2-methylbenzofuran-6-carboxylateHCID 59483316—
SolventWaterHCID 962—
SolventDimethyl EtherHCID 8254—
ProductPf-04937319HCID 46916694—

Reaction Steps

To a solution of the 5-methyl-2-aminopyrazine (38.9 g, 356 mmol) in dimethylether (315 mL) in a 3-neck flask equipped with overhead stirring and a condensor at 0° C. was added Me2AlCl (1 M solution in hexanes) (715 mL). The mixture was warmed at room temperature and stirred for 1.5 hours. In a separate flask, ethyl 4-(2-(dimethylcarbamoyl)pyrimidin-5-yloxy)-2-methylbenzofuran-6-carboxylate (I-2a: 52.6 g, 142.5 mmol) was dissolved in dimethylether (210 mL). This mixture was then added to the complexed amine. A gum precipitated upon scratching the flask and dissipated into a solid. The resultant reaction was refluxed for 3.5 hours HPLC indicated 93% complete. Five liters of Rochelles salt made up in water and 2 liters of 2-methyltetrahydrofuran was added to the mixture. The reaction mixture was then poured into the biphasic system. The mixture was allowed to stir with overhead stirring for 14 hours, after which time, a yellow solid precipitated. The solid was collected through filteration. The solid retained was washed with 2-methyltetrahydrofuran. The resultant solid was dried in vacuo oven overnight to afford the title compound N,N-dimethyl-5-(2-methyl-6-((5-methylpyrazin-2-yl)carbamoyl)benzofuran-4-yloxy)pyrimidine-2-carboxamide (2): (49.98 g, 81%)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08735396B2
Source datasetuspto-grants-2014_05
ORD IDord-078264a94a1c47b0a85572ba465f13f4
Source noteuspto-grants-2014_05