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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2115329Generated: October 26, 2026

Diisopropylethylamine → N-Ethyl-N-pyridin-2-ylmethyl-2-p-tolylamino-acetamide

https://huagongshe.com/reaction/2115329

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
Reactant2-[(4-Methylphenyl)amino]acetic acidHCID 242236—
ReactantO-(Benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborateHCID 2733207—
ReactantN-(pyridin-2-ylmethyl)ethanamineHCID 4723804—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
ProductN-Ethyl-N-pyridin-2-ylmethyl-2-p-tolylamino-acetamideHCID 5897836371.9%

Reaction Conditions

Temperature-20 °C

Reaction Steps

A suspension of ethyl-pyridin-2-ylmethyl-amine (29.0 mmol) and DIPEA (78.0 mmol) in DMF (50 mL) was cooled to −20° C. and added to a cold (−20° C.) solution of p-tolylamino-acetic acid (26.0 mmol) and TBTU (34.0 mmol) in DMF (100 mL). The reaction mixture was stirred for 15 min at −20° C. Water (300 mL) and ethyl acetate (400 mL) were added, the layers were separated and the organic layer washed with water (4×100 mL). The combined aqueous layers were extracted with ethyl acetate (200 mL). The combined organic layers were washed with NaOH solution (1.0 mol/L, 100 mL) and brine (100 mL) and dried with Na2SO4. The solvents were removed in vacuo and the obtained solid was dissolved in ethanol. By addition of a solution of hydrogen chloride in ether a byproduct precipitated which was filtered off. Dilution of the remaining solution with ether led to precipitation of the desired acetamide, which was obtained as a white solid (5.3 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07435815B2
Source datasetuspto-grants-2008_10
ORD IDord-a06c8956e2be4ce19b03bd4dfb655600
Source noteuspto-grants-2008_10