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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2093057Generated: October 26, 2026

4-Methylmorpholine → n-(2-Aminophenyl)-5-(biphenyl-4-ylcarbonyl)-4,5,6,7-tetrahydro[1,3]thiazolo[5,4-c]pyridine-2-carboxamide

https://huagongshe.com/reaction/2093057

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-MethylmorpholineHCID 7972—
Reactant1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimideHCID 15908—
Reactant(1,1'-Biphenyl)-4-carboxylic acidHCID 66724—
Reactant1-HydroxybenzotriazoleHCID 75771—
ReactantN-(2-aminophenyl)-4,5,6,7-tetrahydro[1,3]thiazolo[5,4-c]pyridine-2-carboxamideHCID 58117006—
SolventDimethylformamideHCID 6228—
Productn-(2-Aminophenyl)-5-(biphenyl-4-ylcarbonyl)-4,5,6,7-tetrahydro[1,3]thiazolo[5,4-c]pyridine-2-carboxamideHCID 66865245—

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution of biphenyl-4-carboxylic acid (1.0 mmol) in dry 10 mL DMF, were added 1-hydroxybenzotriazole (1.2 mmol), 1-ethyl-3-(3′-dimethylaminopropyl)carbodiimide (2 mmol) and N-methylmorpholine (2.0 mmol). Solution was cooled to 0° C.N-(2-aminophenyl)-4,5,6,7-tetrahydro[1,3]thiazolo[5,4-c]pyridine-2-carboxamide obtained from step VIII of example 1 (1.1 mmole.) was then added and mixture was stirred at room temperature overnight. Reaction mixture was concentrated, diluted with water, extracted with dichloromethane, washed with brine solution, and dried over anhydrous Na2SO4. Concentrated and purified by column chromatography to yield the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08440830B2
Source datasetuspto-grants-2013_05
ORD IDord-50bf951b9f1b439b8af8161298520a62
Source noteuspto-grants-2013_05