HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1497329Generated: October 30, 2026
Toluene → Ethyl 4-[(2-methoxypyridin-4-yl)methyl]quinoline-2-carboxylate
https://huagongshe.com/reaction/1497329
Participants
| Role | Name | HCID | Charge |
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| Reactant | Toluene | HCID 1140 | — |
| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | 4-(Bromomethyl)-2-methoxypyridine | HCID 19805431 | — |
| Reactant | Ethyl 4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)quinoline-2-carboxylate | HCID 60209908 | — |
| Catalyst | HCID 178418397 | HCID 178418397 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | Ethyl 4-[(2-methoxypyridin-4-yl)methyl]quinoline-2-carboxylate | HCID 60209910 | — |
Reaction Steps
In a microwave vial containing ethyl 4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)quinoline-2-carboxylate (K4) (0.23 g, 0.69 mmol), 4-(bromomethyl)-2-methoxypyridine (M3) (0.17 g, 0.83 mmol), and palladium tetrakis (0.52 g, 0.45 mmol) was, added 4.0 mL toluene, 2.8 mL, ethanol, and 1.0 mL 2.0 M aqueous Na2CO3. The resulting solution was heated to 85° C. for 30 minutes, filtered through Celite, and washed with excess ethyl acetate. The filtrate was washed twice with water, washed with brine, dried over sodium sulfate, filtered, and concentrated. The resultant residue was subjected to silica gel chromatography eluting with 0-100% ethyl acetate in hexanes to afford ethyl 4-[(2-methoxypyridin-4-yl)methyl]quinoline-2-carboxylate (M4) that gave a mass ion (ES+) of 323.3 for M+H+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09199939B2 |
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| Source dataset | uspto-grants-2015_12 |
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| ORD ID | ord-1873c5c5645b4401a0c903f6976f9d9e |
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| Source note | uspto-grants-2015_12 |
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