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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 869948Generated: October 30, 2026

Methanol → HCID 71053007, compound

https://huagongshe.com/reaction/869948

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantEthyl AcetateHCID 8857—
ReactantTrimethylsilyl iodideHCID 85247—
ReactantHCID 68723765HCID 68723765—
SolventAcetonitrileHCID 6342—
ProductHCID 71053007HCID 7105300781.7%

Reaction Conditions

Temperature55 °C

Reaction Steps

To a suspension of 1-(2,3-dihydrobenzofuran-5-yl)-N-(2′-methoxy-3,4-dimethyl-2,3′-bipyridin-6-yl)cyclopropanecarboxamide (105 mg, 0.25 mmol) in CH3CN (5.0 mL) was added TMSI (71.7 μL, 0.50 mmol) drop wise. The reaction was stirred at 55° C. for 1 hour. Methanol (1.0 mL) was added followed by ethyl acetate (6 mL). The organic layer was washed with NaHSO3 (2×), and brine (1×). The organic layer was dried over Na2SO4, filtered and evaporated under reduced pressure. The crude product was purified by column chromatography on silica gel (0-10% methanol in dichloromethane) to yield 1-(2,3-dihydrobenzofuran-5-yl)-N-(4,5-dimethyl-6-(2-oxo-1,2-dihydropyridin-3-yl)pyridin-2-yl)cyclopropanecarboxamide as a white solid (82 mg, 81%). ESI-MS m/z calc. 401.5. found 402.5 (M+1)+. Retention time 1.18 minutes.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08969386B2
Source datasetuspto-grants-2015_03
ORD IDord-a90cdfc332f74b54bbaece2eda18ede4
Source noteuspto-grants-2015_03