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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2170444Generated: October 30, 2026

Trimethylsilyl iodide → HCID 86728490, compound

https://huagongshe.com/reaction/2170444

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrimethylsilyl iodideHCID 85247—
ReactantHCID 86728489HCID 86728489—
SolventAcetonitrileHCID 6342—
ProductHCID 86728490HCID 8672849013%

Reaction Conditions

Temperature50 °C

Reaction Steps

To the 4-(tert-butyl)-N-(2-methoxypyridin-4-yl)-2-((6-(trifluoromethyl)pyridin-3-yl)oxy)benzamide (137 mg, 0.3 mmol) in acetonitrile (4.9 mL) was added TMSI (93.3 μL, 0.66 mmol). The reaction was stirred at 50° C. for 12 hours. The reactions was cooled to 25° C., filtered and purified by reverse phase HPLC (10-99% ACN in Water with HCl as a modifier) to yield 4-(tert-butyl)-N-(2-oxo-1,2-dihydropyridin-4-yl)-2-((6-(trifluoromethyl)pyridin-3-yl)oxy)benzamide (141) (14.4 mg, 13%). ESI-MS m/z calc. 431.15. found 432.3 (M+1)+; Retention time: 1.78 minutes (3 minutes run).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09051270B2
Source datasetuspto-grants-2015_06
ORD IDord-4d0949d167914d70997d112aea8b686e
Source noteuspto-grants-2015_06