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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1293370Generated: October 29, 2026

Trimethylsilyl iodide → 5'-Chloro-4-methyl-3,4,5,6-tetrahydro-2H-(1,2')bipyridinyl-4-ylamine

https://huagongshe.com/reaction/1293370

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrimethylsilyl iodideHCID 85247—
Reactant(5'-chloro-4-methyl-3,4,5,6-tetrahydro-2H-(1,2')bipyridinyl-4-yl)-carbamic acid benzyl esterHCID 66756881—
SolventAcetonitrileHCID 6342—
Product5'-Chloro-4-methyl-3,4,5,6-tetrahydro-2H-(1,2')bipyridinyl-4-ylamineHCID 17860829—

Reaction Conditions

Temperature50 °C

Reaction Steps

To a stirred solution of (5′-chloro-4-methyl-3,4,5,6-tetrahydro-2H-(1,2′)bipyridinyl-4-yl)-carbamic acid benzyl ester (0.060 g, 0.17 mmol ) in acetonitrile (1.0 mL) at room temperature was added iodotrimethysilane (0.04 mL, 0.25 mmol). The reaction mixture was stirred at 50° C. for 30 minutes, concentrated under reduced pressure, and purified by flash chromatography with 3% methanol in dichloromethane to provide titled compound. MS (CI) m/z 226 (M+1)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07238724B2
Source datasetuspto-grants-2007_07
ORD IDord-e5dc0d6833924327bd170a5fd5e380c1
Source noteuspto-grants-2007_07