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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 365912Generated: October 25, 2026

Potassium Carbonate → 3-(1-Boc-2-(s)-pyrrolidinylmethoxy)-6-chloro-5-methylpyridine

https://huagongshe.com/reaction/365912

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant6-Chloro-5-methylpyridin-3-yl acetateHCID 21828869—
Reactant1-BOC-2-(S)-methyltoluenesulfonate pyrrolidineHCID 131722021—
SolventMethanolHCID 887—
Product3-(1-Boc-2-(s)-pyrrolidinylmethoxy)-6-chloro-5-methylpyridineHCID 2296184046.2%

Reaction Steps

To a solution of 5-acetoxy-2-chloro-3-methylpyridine (1.80 g, 8.9 mmol) in MeOH (5 mL) was added potassium carbonate (1.4 g, 10.1 mmol). The reaction mixture was allowed to stir at room tenperature for 2.5 h. Solvent was evaporated. The residue was then dissolved in DMF, and 1-BOC-2-(S)-methyltoluenesulfonate-pyrrolidine (2.0 g, 5.63 mmol) from a above was added. The reaction mixture was stirred at 60° C. for 16 h. Solvent was evaporated. The residue was chromatographed (silica gel; hexane/EtOAc, 10:1 to 3:1) to afford an oil (850 mg, 30%): 1H NMR δ 1.47 (s, 9H), 1.80-2.00 (m, 2H), 2.00-2.08 (m, 2H), 2.34 (s, 3H), 3.24-3.44 (m, 2H), 3.92 (m, 1H), 4.02-4.20 (m, 2H), 7.16 (m, 1H), 7.92 (d, 1H, J=2.5 Hz); MS (CI/NH3) m/z 227 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06127386
Source datasetuspto-grants-2000_10
ORD IDord-63fd7c10c4ba43279e2579e8e88b92b3
Source noteuspto-grants-2000_10