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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1039741Generated: October 26, 2026

Triethylamine → 2-Methoxy-4-methyl-6-morpholin-4-yl-pyridine-3-carboxylic acid

https://huagongshe.com/reaction/1039741

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant3,5-DifluorobenzylamineHCID 145211—
Reactant6-Chloro-2-methoxy-4-methylpyridine-3-carboxylic acidHCID 707652—
ReactantMethanaminium, N-((dimethylamino)(3H-1,2,3-triazolo(4,5-b)pyridin-3-yloxy)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1)HCID 9886157—
SolventTetrahydrofuranHCID 8028—
SolventEthyl AcetateHCID 8857—
Product2-Methoxy-4-methyl-6-morpholin-4-yl-pyridine-3-carboxylic acidHCID 6728664154%

Reaction Conditions

Temperature50 °C

Reaction Steps

To a solution of 302 mg crude 6-chloro-2-methoxy-4-methyl-pyridine-3-carboxylic acid in THF (12 ml) were added 568 mg (1.5 mmol) HATU and 934 μl (6.8 mmol) NEt3. The RM was stirred at 50° C. for 3 h followed by the addition of 268 mg (1.9 mmol) 3,5-difluorobenzylamine. Stirring was continued at 50° C. for 72 h. The RM was then diluted with EtOAc (50 ml) and subsequently washed with a 4M aq. NH4Cl sol., a 1M aq. NaHCO3 sol. and brine. The organic layer was dried over MgSO4 and concentrated in vacuo. Purification of the residue by CC (hexane/EtOAc 3:1) provided 237 mg (0.7 mmol, 54% over 2 steps) 2-methoxy-4-methyl-6-morpholin-4-yl-pyridine-3-carboxylic acid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08552200B2
Source datasetuspto-grants-2013_10
ORD IDord-e5af66282fdb41c8aed9a20e95e82396
Source noteuspto-grants-2013_10