HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 747652Generated: October 29, 2026
HCID 55285521, compound → HCID 59749717, compound
https://huagongshe.com/reaction/747652
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | HCID 55285521 | HCID 55285521 | — |
| Reactant | 167980-35-0 | HCID 59749716 | — |
| Reactant | HCID 69137611 | HCID 69137611 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 59749717 | HCID 59749717 | — |
Reaction Steps
Ethyl 3-amino-5-(4-fluorophenyl)-2-pentenoate 4 (119 mg, 0.5 mmol), 4-formyl-N-pyridin-3-ylmethyl-benzamide 8 (120 mg, 0.5 mmol) and 3-Imino-5-methyl-hexanoic acid amide 11 (92 mg, 0.65 mmol) were dissolved in EtOH (4 mL). The reaction was stirred at 120° C. overnight. The crude reaction mixture was purified via reverse phase LC/MS to yield, 29 mg of target material. The compound was characterized by NMR and LC/MS. 1H NMR (500 MHz, CDCl3): δ 8.79 (s, 1H), 8.51 (d, J=4.7 Hz, 1H), 8.29 (d, J=7.9 Hz, 1H), 7.68 (m, 4H), 7.28 (d, J=8.5 Hz, 1H), 7.08 (m, 2H), 6.90 (m, 2H), 4.63 (br. s, 2H), 4.04 (q, J=6.8 Hz, 2H), 3.37 (s, 1H), 2.86 (q, J=7.2 Hz, 2H), 2.78 (m, 3H), 2.50 (m, 1H), 1.65 (m, 1H), 1.17 (t, J=6.7 Hz, 3H), 0.82 (t, J=6.9 Hz, 6H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07396936B1 |
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| Source dataset | uspto-grants-2008_07 |
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| ORD ID | ord-36fd75c82774475896d84d44d8744887 |
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| Source note | uspto-grants-2008_07 |
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