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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 3-Isopropyl acrylic acid | HCID 642039 | — |
| Reactant | Methanaminium, N-((1H-benzotriazol-1-yloxy)(dimethylamino)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1) | HCID 2733084 | — |
| Reactant | N1-(2-Methylquinolin-4-yl)ethane-1,2-diamine | HCID 6471895 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | (E)-N-[2-[(2-Methyl-4-quinolyl)amino]ethyl]but-2-enamide | HCID 86691181 | 68.3% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08877934B2 |
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| Source dataset | uspto-grants-2014_11 |
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| ORD ID | ord-5f64f7331f114d09a892ddee5f9bd4b8 |
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| Source note | uspto-grants-2014_11 |
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