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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2079959Generated: October 27, 2026

Triethylamine → 6-amino-N-(5-(3-fluoro-phenoxy)-thiophen-2-yl)-methylnicotinamide

https://huagongshe.com/reaction/2079959

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant6-Aminonicotinic acidHCID 18496—
ReactantBenzotriazol-1-yltris(dimethylamino)phosphonium hexafluorophosphateHCID 10938826—
ReactantC-(5-(3-fluorophenoxy)thiophen-2-yl)methylamineHCID 23130606—
SolventMethanolHCID 887—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
Product6-amino-N-(5-(3-fluoro-phenoxy)-thiophen-2-yl)-methylnicotinamideHCID 2313057543.9%

Reaction Conditions

Temperature60 °C

Reaction Steps

To a solution of 6-amino-nicotinic acid (270 mg, 2.0 mmol) and C-(5-(3-fluorophenoxy)thiophen-2-yl)methylamine (400 mg, 1.8 mmol) in N,N-dimethylformamide (10 mL) were added benzotriazole-1-yl-tris(dimethylamino)phosphonium hexafluorophosphate (870 mg, 2.0 mmol) and triethylamine (0.50 mL, 3.6 mmol), and the solution was stirred for 30 minutes at 60° C. Water and ethyl acetate were added to the reaction solution, which was then partitioned, and the organic layer was washed twice with water. Silica gel was added to the organic layer, the solvent was evaporated in vacuo for adsorption, purification was carried out with NH silica gel column chromatography (ethyl acetate, then ethyl acetate:methanol=10:1), and 6-amino-N-(5-(3-fluoro-phenoxy)-thiophen-2-yl)-methylnicotinamide (270 mg, 0.79 mmol, 43.9%) was obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07932272B2
Source datasetuspto-grants-2011_04
ORD IDord-c34d88ad764542a390acfddc6744389b
Source noteuspto-grants-2011_04