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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 970914Generated: October 31, 2026

Triethylamine → HCID 20747308, compound

https://huagongshe.com/reaction/970914

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant2,4-Dimethyl-3-pyridinecarboxylic acidHCID 1512561—
ReactantHCID 9887073HCID 9887073—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventThionyl ChlorideHCID 24386—
ProductHCID 20747308HCID 2074730843.3%

Reaction Steps

A solution of 2,4-dimethyl-nicotinic acid (56 mg, 0.37 mmol) in SOCl2 (˜3 mL, excess) was heated to 80° C. for 4 hours. The condenser was removed and the mixture was flushed with N2 at 80° C. for ˜5 minutes and then dried in vacuo for 10 minutes. The resulting syrup was dissolved in CH2Cl2 (2.0 mL) and added to a stirring mixture of (3-aminomethyl-benzyl)-(1H-benzoimidazol-2-ylmethyl)-(5,6,7,8-tetrahydro-quinolin-8-yl)-amine (147 mg, 0.37 mmol), Et3N (0.26 mL, 1.85 mmol) and a catalytic amount of DMAP. The reaction mixture was stirred ovemight at room temperature. Purification of the crude yellow foam by column chromatography on silica gel (CH2Cl2/MeOH/NH4OH, 100:1:1) followed by radial chromatography on silica gel (1 mm plate, EtOAc/MeOH/NH4OH, 200:1:1) afforded the desired amide (85 mg, 43%) as a light yellow foam.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07312234B2
Source datasetuspto-grants-2007_12
ORD IDord-e7edc77f52624170a97b1e468e8dc5ee
Source noteuspto-grants-2007_12