HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 843147Generated: October 30, 2026
3-Pyridinemethanamine → HCID 86757971, compound
https://huagongshe.com/reaction/843147
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 3-Pyridinemethanamine | HCID 31018 | — |
| Reactant | HCID 54533680 | HCID 54533680 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Solvent | N-methyl-2-pyrrolidone | HCID 13387 | — |
| Product | HCID 86757971 | HCID 86757971 | — |
Reaction Steps
4-(3-Bromo-propoxy)-3-methyl-benzofuran-2-carboxylic acid (2-cyclohexyl-ethyl)-amide (100 mg) and 3-picolyl amine (250 μl) were dissolved in 1-methylpyrrolidone (2 ml) and heated at 100° C. for two hours. The reaction mixture was dissolved in ethyl acetate and washed with saturated ammonium chloride solution and water. The organic solvent was dried over anhydrous sodium sulfate and evaporated to dryness. The residue was purified by silica gel column chromatography (dichloromethane-MeOH) to afford 3-methyl-4-{3-[(pyridin-3-ylmethyl)-amino]-propoxy}-benzofuran-2-carboxylic acid (2-cyclohexyl-ethyl)-amide. ESI-MS: m/z 450 (MH+); 1H-NMR (CDCl3): δ 0.85-1.85 (13H, m), 2.05 (2H, quintet, J=6.5 Hz), 2.72 (3H, s), 2.90 (2H, t, J=6.5 Hz), 3.46 (2H, m), 3.85 (2H, s), 4.15 (2H, t, J=6.5 Hz), 6.53 (1H, t, J=6 Hz), 6.62 (1H, d, 8 Hz), 7.01 (1H, d, J=8 Hz), 7.26 (2H, m), 7.68 (1H, dd, J=1.5 Hz, 8 Hz), 8.49 (1H, br d, J=3.5 Hz), 8.56 (1H, br s).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06376491B1 |
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| Source dataset | uspto-grants-2002_04 |
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| ORD ID | ord-bd5d5bce33e148718de73449c6d0c42f |
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| Source note | uspto-grants-2002_04 |
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