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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 870006Generated: October 31, 2026

Trimethylsilyl iodide → HCID 68737441, compound

https://huagongshe.com/reaction/870006

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrimethylsilyl iodideHCID 85247—
ReactantHCID 68722356HCID 68722356—
SolventMethanolHCID 887—
ProductHCID 68737441HCID 6873744142.1%

Reaction Conditions

Temperature55 °C

Reaction Steps

To a slurry of 1-(2,3-dihydrobenzofuran-6-yl)-N-(6′-methoxy-4-methyl-2,3′-bipyridin-6-yl)cyclopropanecarboxamide (20 mg, 0.049 mmol) in acetonitrilee (1.5 mL) was added TMS-I (28.4 μL, 0.19 mmol) and the mixture was stirred at 55° C. for 7 h. The reaction was diluted with methanol (1.0 mL) and stirred at room temperature for 2 h. The resulting mixture was concentrated under vacuum, and taken into ethyl acetate (10 mL). The organic solution was washed with sodium bisulphate (2×2 ml), water (2×3 mL), dried over sodium sulphate and concentrated under vacuum. The solid was stirred with methanol (1.0 mL) at 40° C. for 10 min and collected by filtration, washed with methanol (1.0 mL) and dried under vacuum to yield the product (8.0 mg, 41%). ESI-MS m/z calc. 387.4. found 388.2 (M+1)+. Retention time 1.44 minutes.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08969386B2
Source datasetuspto-grants-2015_03
ORD IDord-c1122fd219de4abdb7baa086574c7141
Source noteuspto-grants-2015_03