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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 877373Generated: October 30, 2026

Triethylamine → HCID 67165955, compound

https://huagongshe.com/reaction/877373

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant2-Amino-2-phenylacetonitrile hydrochlorideHCID 40837—
Reactant4-Isopropylphenylacetic acidHCID 78230—
ReactantHOAtHCID 181649—
Reactant1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
ProductHCID 67165955HCID 6716595554.6%

Reaction Steps

To a 100 ml round bottom flask equipped with a magnetic stir bar were added 4-isopropylphenylacetic acid (1.786 g, 10.02 mmol), cyano(phenyl)-methanaminium chloride (1.690 g, 10.02 mmol), 1-(3-dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride (1.921 g, 10.02 mmol), 1-hydroxy-7-azabenzotriazole (1.364 g, 10.02 mmol) and triethylamine (3.042 ml, 30.06 mmol) into 30.0 ml of CH2Cl2. The resulting solution was stirred at room temperature for 16 hours. The reaction mixture was diluted with water and the two layers were separated. The aqueous layer was extracted with CH2Cl2. The combined organic layers were washed with brine, dried over anhydrous Na2SO4 and filtered. The filtrate was concentrated in vacuum. Purification by preparative HPLC (20-90% CH3CN/H2O over 30 min, 0.05% added TFA, C18 column) to afford 1.6 g (54%) of the title compound. 1H NMR (CDCl3, 400 MHz) δ 7.382 (m, 5H), 7.206 (m, 4H), 6.156 (d, J=8.6 Hz, 1H), 5.997 (br d, J=8.2 Hz, 1H), 3.632 (s, 2H), 2.895 (sept, J=7.0 Hz, 1H), 1.238 (d, J=7.0 Hz, 6H). ES-MS [M+1]+: 293.2.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08987310B2
Source datasetuspto-grants-2015_03
ORD IDord-5466ea500c90474dae7bb2bb9e1f4a32
Source noteuspto-grants-2015_03