Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2420928Generated: November 1, 2026

Trimethylsilyl iodide → HCID 178426546, compound

https://huagongshe.com/reaction/2420928

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrimethylsilyl iodideHCID 85247—
Reactant1-(2,2-difluorobenzo[d][1,3]dioxol-5-yl)-N-(6-(2-methoxypyrimidin-5-yl)-5-methylpyridin-2-yl)cyclopropanecarboxamideHCID 59165850—
SolventAcetonitrileHCID 6342—
ProductHCID 178426546HCID 178426546—

Reaction Conditions

Temperature75 °C

Reaction Steps

To a solution of 1-(2,2-difluorobenzo[d][1,3]dioxol-5-yl)-N-(6-(2-methoxypyrimidin-5-yl)-5-methylpyridin-2-yl)cyclopropanecarboxamide (88 mg, 0.20 mmol) in CH3CN (2 mL) was added TMSI (80 mg, 0.40 mmol). The mixture was heated at 75° C. for 4 hours. The mixture was partitioned between ethyl acetate and H2O, and the aqueous layer was extracted with ethyl acetate (3×). The combined organic layers were washed with brine, dried over MgSO4, and concentrated under reduced pressure. The residue was purified by preparative LC/MS to yield 1-(2,2-difluorobenzo[d][1,3]dioxol-5-yl)-N-(6-(2-hydroxypyrimidin-5-yl)-5-methylpyridin-2-yl)cyclopropanecarboxamide. MS (ESI) m/e (M+H+) 427.3.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07956052B2
Source datasetuspto-grants-2011_06
ORD IDord-187f513d717b4ba687d71d2817c3b21d
Source noteuspto-grants-2011_06