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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 922055Generated: October 31, 2026

(3-Methoxy-1-propynyl)tributylstannane → 2-(3-Methoxyprop-1-ynyl)-4-methyl-6-morpholino-pyridine-3-carboxylic acid methylester

https://huagongshe.com/reaction/922055

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(3-Methoxy-1-propynyl)tributylstannaneHCID 10872067—
Reactant2-Chloro-4-methyl-6-morpholino-pyridine-3-carboxylic acid methylesterHCID 86664331—
CatalystHCID 178418476HCID 178418476—
Solvent1,4-DioxaneHCID 31275—
Product2-(3-Methoxyprop-1-ynyl)-4-methyl-6-morpholino-pyridine-3-carboxylic acid methylesterHCID 8666433263.1%

Reaction Conditions

Temperature100 °C

Reaction Steps

To a solution of 700 mg (2.6 mmol) 2-chloro-4-methyl-6-morpholino-pyridine-3-carboxylic acid methylester and 1.39 g (3.9 mmol) tributyl(3-methoxyprop-1-ynyl)stannane in dioxane (10 ml) was added 273 mg (0.39 mmol) PdCl2(PPh3)2. Then the reaction solution was heated at 100° C. for 16 h. After cooling to RT the mixture was filtered through celite and the filtrate was concentrated in vacuo. The residue was dissolved in EtOAc and washed with water. The organic layer was dried over Na2SO4 and concentrated in vacuo. Purification of the residue by CC (5% KF-silica, hexane/EtOAc 19:1) provided 500 mg (1.64 mmol, 63%) 2-(3-methoxyprop-1-ynyl)-4-methyl-6-morpholino-pyridine-3-carboxylic acid methylester.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09278103B2
Source datasetuspto-grants-2016_03
ORD IDord-d0e3f87a73614e2284a6ca500ff8af16
Source noteuspto-grants-2016_03