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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1963859Generated: November 1, 2026

Dimethyl Sulfoxide → Tert-butyl 4-(5-chloro-4-iodopyridin-2-yl-amino)piperidine-1-carboxylate

https://huagongshe.com/reaction/1963859

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethyl SulfoxideHCID 679—
Reactant4-Amino-1-Boc-piperidineHCID 1268291—
Reactant5-Chloro-2-fluoro-4-iodopyridineHCID 21865336—
SolventEthyl AcetateHCID 8857—
ProductTert-butyl 4-(5-chloro-4-iodopyridin-2-yl-amino)piperidine-1-carboxylateHCID 6693696966.6%

Reaction Conditions

Temperature90 °C

Reaction Steps

A mixture of 5-chloro-2-fluoro-4-iodopyridine (517 mg, 2.008 mmol), tert-butyl 4-aminopiperidine-1-carboxylate (603 mg, 3.01 mmol), DMSO (2 ml) and TEA (0.420 ml, 3.01 mmol) reaction mixture was stirred at 90° C. for 18 hours. The reaction mixture was cooled to room temperature, mixed with 150 ml of ethyl acetate, washed with saturated sodium bicarbonate (2×), water (3×), saturated salt solution (1×), dried sodium sulfate, filtered and concentrated to yield a crude material, which was purified by silica gel chromatography using a 40 g column, eluting from 0%-40% ethyl acetate with hexane. The desired fractions were concentrated to constant mass, giving 585 mg of the title compound as free base. LCMS (m/z): 438.1 (MH+), retention time=1.00 min.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08415381B2
Source datasetuspto-grants-2013_04
ORD IDord-72d8d5a861b249468747b1ca029d3f0f
Source noteuspto-grants-2013_04