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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1497327Generated: October 30, 2026

Trimethylsilyl iodide → HCID 178523840, compound

https://huagongshe.com/reaction/1497327

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrimethylsilyl iodideHCID 85247—
ReactantHCID 53307628HCID 53307628—
SolventDichloromethaneHCID 6344—
ProductHCID 178523840HCID 178523840—

Reaction Conditions

Temperature50 °C

Reaction Steps

To a solution of N-[(3R,4S)-3-Hydroxytetrahydro-2H-pyran-4-yl]-4-[(6-methoxypyridin-3-yl)methyl]quinoline-2-carboxamide (0.15 g, 0.38 mmol) in CH2Cl2 was added trimethylsilyl iodide (0.15 mL, 1.1 mmol). The reaction mixture was heated to 50° C. for 16 h and cooled to room temperature and concentrated. The resultant residue was subjected to silica gel chromatography eluting with 0-15% methanol in methylene chloride to afford 4-[(6-hydroxypyridin-3-yl)methyl]-N-[(3R,4S)-3-hydroxytetrahydro-2H-pyran-4-yl]quinoline-2-carboxamide (L1) that gave a mass ion (ES+) of 380.4 for M+H+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09199939B2
Source datasetuspto-grants-2015_12
ORD IDord-9029c5a627dc4999b15d980882fe61bd
Source noteuspto-grants-2015_12