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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | 2-[(4-Methylphenyl)amino]acetic acid | HCID 242236 | — |
| Reactant | O-(Benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborate | HCID 2733207 | — |
| Reactant | N-(pyridin-2-ylmethyl)ethanamine | HCID 4723804 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | N-Ethyl-N-pyridin-2-ylmethyl-2-p-tolylamino-acetamide | HCID 58978363 | 71.9% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07435815B2 |
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| Source dataset | uspto-grants-2008_10 |
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| ORD ID | ord-a06c8956e2be4ce19b03bd4dfb655600 |
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| Source note | uspto-grants-2008_10 |
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