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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 264282Generated: October 30, 2026

3-(Chloromethyl)pyridine hydrochloride → HCID 10551450, compound

https://huagongshe.com/reaction/264282

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-(Chloromethyl)pyridine hydrochlorideHCID 23394—
ReactantSodium hydrideHCID 24758—
ReactantN-[4-methoxybenzenesulfonyl]-(D)-leucine t-butyl esterHCID 10808269—
SolventDimethylformamideHCID 6228—
ProductHCID 10551450HCID 10551450—

Reaction Steps

To a solution of t-butyl 2(R)-[[4-methoxybenzenesulfonyl]amino]-4-methylpentanoate (10.0 g, 27.92 mmol) in dimethylformamide (250 mL) at room temperature is added 3-picolyl chloride hydrochloride (4.81 g, 29.32 mmol) followed by sodium hydride (2.79 g, 69.80 mmol, 60% in oil). The reaction mixture is stirred at room temperature for 48 hours. The mixture is quenched with water and extracted with ethyl acetate. The combined organic extracts are washed with brine, dried (Na2SO4), and the solvent is evaporated. The crude product is purified by silica gel chromatography (45% ethyl acetate/hexanes) to provide t-butyl 2(R)-[[4-methoxybenzenesulfonyl](3-picolyl)-amino]-4-methylpentanoate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05646167
Source datasetuspto-grants-1997_07
ORD IDord-ad7680e8bb6442b1a1807e04b3789172
Source noteuspto-grants-1997_07