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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2079961Generated: October 31, 2026

Triethylamine → 6-amino-N-(5-benzylthiophen-2-ylmethyl)-nicotinamide

https://huagongshe.com/reaction/2079961

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant6-Aminonicotinic acidHCID 18496—
ReactantBenzotriazol-1-yltris(dimethylamino)phosphonium hexafluorophosphateHCID 10938826—
Reactant2-Thiophenemethanamine,5-(phenylmethyl)-HCID 23130612—
SolventMethanolHCID 887—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
Product6-amino-N-(5-benzylthiophen-2-ylmethyl)-nicotinamideHCID 2313035329.5%

Reaction Conditions

Temperature60 °C

Reaction Steps

To a solution of 6-aminonicotinic acid (340 mg, 2.4 mmol) and C-(5-benzyl-thiophen-2-yl)-methylamine described in Preparation Example 42 (450 mg, 2.2 mmol) in N,N-dimethylformamide (5 mL) were added benzotriazol-1-yl-tris(dimethylamino)phosphonium hexafluorophosphate (1.1 g, 2.4 mmol) and triethylamine(0.62 mL, 4.4 mmol), and the solution was stirred at 60° C. for 1 hour. 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 adsorption, purification was carried out by NH silica gel column chromatography (hexane:ethyl acetate=1:1, then ethyl acetate, then ethyl acetate:methanol=10:1), and 6-amino-N-(5-benzyl-thiophen-2-ylmethyl)-nicotinamide (210 mg, 0.65 mmol, 29.5%) was obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07932272B2
Source datasetuspto-grants-2011_04
ORD IDord-07255c3963894ecca90e46bbafeb493a
Source noteuspto-grants-2011_04