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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2079982Generated: October 30, 2026

Triethylamine → Quinoline-6-carboxylic acid cyanomethyl-amide

https://huagongshe.com/reaction/2079982

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant6-Quinolinecarboxylic acidHCID 82571—
ReactantBenzotriazol-1-yltris(dimethylamino)phosphonium hexafluorophosphateHCID 10938826—
ReactantAminoacetonitrile hydrochlorideHCID 11491918—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
ProductQuinoline-6-carboxylic acid cyanomethyl-amideHCID 5838807869%

Reaction Conditions

Temperature60 °C

Reaction Steps

To a solution of quinoline-6-carboxylic acid (500 mg, 2.9 mmol) and amino acetonitrile hydrochloride (320 mg, 3.4 mmol) in N,N-dimethylformamide (10 mL) were added benzotriazol-1-yl-tris(dimethylamino)phosphonium hexafluorophosphate (1.5 g, 3.48 mmol) and triethylamine (1.2 mL, 8.7 mmol), and the solution was stirred at 60° C. for 10 minutes. Ethyl acetate and water was added to the reaction solution, which was then partitioned, the organic layer was washed twice with water. Silica gel was added to the organic layer, the solvent was evaporated in vacuo for adsorption, purified by NH silica gel column chromatography (ethyl acetate), and the title compound (420 mg, 2.0 mmol, 68.9%) was obtained as a light brown solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07932272B2
Source datasetuspto-grants-2011_04
ORD IDord-03ffffbe175744569397c4bac26ba816
Source noteuspto-grants-2011_04