HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 333923Generated: October 30, 2026
HCID 10910039, compound → HCID 57413701, compound
https://huagongshe.com/reaction/333923
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | HCID 10910039 | HCID 10910039 | — |
| Reactant | HCID 68008562 | HCID 68008562 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Product | HCID 57413701 | HCID 57413701 | — |
Reaction Steps
A solution of 5-(4-(dimethylamino)phenyl)-3-methylpyridin-2-amine (120b, 2.27 g, 10.0 mmol) in pyridine (30 ml) was added with 3-(5-methylfuran-2-yl)propanoyl chloride (1.90 g, 11.0 mmol) and then stirred at room temperature for further 16 hours. The reaction mixture was quenched with water and extracted with ethyl acetate. The organic layer was washed with brine, dried over MgSO4(s) and concentrated under reduced pressure. The residue was purified by column chromatography on silica gel to give N-(5-(4-(Dimethylamino)phenyl)-3-methylpyridin-2-yl)-3-(5-methylfuran-2-yl) propanamide (120): 1H NMR (500 MHz, DMSO-d6):δ: 9.99 (s, 1H), 8.46 (s, 1H), 7.84 (s, 1H), 7.55 (m, 2H), 6.81 (m, 2H), 5.98 (s, 1H), 5.94 (s, 1H), 2.94 (s, 6H), 2.87 (t, 2H), 2.65 (t, 2H), 2.21 (s, 3H), 2.16 (s, 3H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08883793B2 |
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| Source dataset | uspto-grants-2014_11 |
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| ORD ID | ord-d9e3e06a13b840c6bcb9ed4cb0183c60 |
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| Source note | uspto-grants-2014_11 |
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