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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 333098Generated: October 30, 2026

Triethylamine → (E)-N-[2-[(2-Methyl-4-quinolyl)amino]ethyl]but-2-enamide

https://huagongshe.com/reaction/333098

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant3-Isopropyl acrylic acidHCID 642039—
ReactantMethanaminium, N-((1H-benzotriazol-1-yloxy)(dimethylamino)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1)HCID 2733084—
ReactantN1-(2-Methylquinolin-4-yl)ethane-1,2-diamineHCID 6471895—
SolventAcetonitrileHCID 6342—
Product(E)-N-[2-[(2-Methyl-4-quinolyl)amino]ethyl]but-2-enamideHCID 8669118168.3%

Reaction Conditions

Temperature0 °C

Reaction Steps

(E)-4-Methylpent-2-enoic acid (190 mg, 1.3 mmol) was mixed together with HBTU (470 mg, 1.3 mmol) and N-(2-methyl-4-quinolyl)ethane-1,2-diamine (250 mg, 1.2 mmol) in acetonitrile (5 ml). Triethylamine (1 mll) was added with stirring at 0° C. over 15 minutes and the resulting mixture was stirred at room temperature overnight. The volatiles were removed under reduced pressure, the residue was dissolved in DCM and washed with a saturated solution of sodium bicarbonate. The combined aqueous solutions were extracted three times with DCM. The organic layers were combined, dried over sodium sulfate, the solvent was removed under reduced pressure to give 245 mg of a yellow solid (0.82 mmol, 66%). MS (APCI) m/z=298.2 [M+1]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08877934B2
Source datasetuspto-grants-2014_11
ORD IDord-5f64f7331f114d09a892ddee5f9bd4b8
Source noteuspto-grants-2014_11