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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 922057Generated: October 31, 2026

Potassium Phosphate, Tribasic → 2-Cyclopropyl-4-methyl-6-morpholino-pyridine-3-carboxylic acid methylester

https://huagongshe.com/reaction/922057

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium Phosphate, TribasicHCID 62657—
ReactantTricyclohexylphosphineHCID 75806—
ReactantCyclopropylboronic acidHCID 2760897—
Reactant2-Chloro-4-methyl-6-morpholino-pyridine-3-carboxylic acid methylesterHCID 86664331—
Catalystpalladium(II) acetateHCID 167845—
SolventWaterHCID 962—
SolventTolueneHCID 1140—
Product2-Cyclopropyl-4-methyl-6-morpholino-pyridine-3-carboxylic acid methylesterHCID 8666433480%

Reaction Conditions

Temperature120 °C

Reaction Steps

To a solution of 1.0 g (3.69 mmol) 2-chloro-4-methyl-6-morpholino-pyridine-3-carboxylic acid methylester (synthesis is described in section b) of example 354) in toluene (20 ml) were added 634 mg (7.38 mmol) cyclopropyl boronic acid, 2.74 g (12.9 mmol) K3PO4, 104 mg (0.37 mmol) tri-cyclohexyl-phosphine and water (1 ml). After degassing for 30 min 82 mg (0.37 mmol) Pd(OAc)2 were added and the reaction solution was heated at 120° C. for 16 h. The mixture was then poured into water and extracted with EtOAc. The organic layer was washed with water and brine, dried over Na2SO4 and concentrated in vacuo. Purification of the residue by CC (hexane/EtOAc 17:3) provided 500 mg (1.84 mmol, 80%) 2-cyclopropyl-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-6b96c68187cf4d39b15ff697928238c3
Source noteuspto-grants-2016_03