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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1099437Generated: October 26, 2026

Triethylamine → HCID 59354919, compound

https://huagongshe.com/reaction/1099437

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant5-(Methoxycarbonyl)pyridine-2-carboxylic acidHCID 314992—
ReactantMethanaminium, N-((1H-benzotriazol-1-yloxy)(dimethylamino)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1)HCID 2733084—
Reactant3,3,3-Trifluoropropylamine hydrochlorideHCID 25210505—
SolventAcetonitrileHCID 6342—
ProductHCID 59354919HCID 5935491925%

Reaction Steps

5-(methoxycarbonyl)pyridine-2-carboxylic acid (100 mg, 0.55 mmol) was dissolved in acetonitrile (1 mL). Triethylamine (0.230 mL, 1.66 mmol) and O-benzotriazol-1-yl-tetramethyluronium hexafluorophosphate (314 mg, 0.83 mmol) were added. The reaction mixture was stirred at rt for 5 min. 3,3,3-trifluoropropylamine hydrochloride (83 mg, 0.55 mmol) was added and the reaction mixture was stirred at ambient temperature for 2 h. The solvent was removed in vacuo and the crude was pardoned between ethyl acetate and 1M sodium hydroxide. The organic layer was dried over magnesium sulfate and concentrated in vacuo. The crude was purified by column chromatography using a gradient of ethyl acetate in heptane yielded 38 mg (25%) of the title compound as a white solid; 1H NMR (400 MHz, DMSO-d6) δ ppm 9.17 (t, 1 H), 9.11 (d, 1 H), 8.48 (dd, 1 H), 8.18 (d, 1 H), 3.92 (s, 3 H), 3.53-3.60 (m, 2 H), 2.54-2.66 (m, 2 H); MS (ESI) m/z 277[M+H+], m/z 275[M−H+];

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08143408B2
Source datasetuspto-grants-2012_03
ORD IDord-318c1becbabf4afdbf5581d0337ba3b8
Source noteuspto-grants-2012_03