HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1250490Generated: October 31, 2026
M-Cresol → N-(4-methylphenyl)-4-methoxy-6-(3-methylphenoxy)-2-pyridine carboxamide
https://huagongshe.com/reaction/1250490
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | M-Cresol | HCID 342 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | N-(4-methylphenyl)-6-bromo-4-methoxy-2-pyridine carboxamide | HCID 18326207 | — |
| Catalyst | Cupric Chloride | HCID 24014 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Hexane | HCID 8058 | — |
| Product | N-(4-methylphenyl)-4-methoxy-6-(3-methylphenoxy)-2-pyridine carboxamide | HCID 15906600 | — |
Reaction Steps
0.45 g (0.0019×2.2 mol) of 3-methyl phenol was dissolved in about 10 ml of DMF. The obtained solution was further mixed with 0.15 g (ca. 60% in mineral oil; 0.0019×2.0 mol) of NaH and then with 0.60 g (0.0019 mol) of N-(4-methylphenyl)-6-bromo-4-methoxy-2-pyridine carboxamide. After adding 0.19 g (0.0019×1.0 mol) of copper chloride (I), the solution was stirred at about 100° C. for about 4 hours, and then allowed to stand for cooling to room temperature. After the reaction solution was distributed in hexane-saturated sodium bicarbonate water, the organic phase of the solution was washed with saturated brine and dried with anhydrous sodium sulfate, followed by concentration thereof. Thereafter, the concentrated solution was purified by silica gel column chromatography (eluting solution: ethyl acetate/hexane), thereby obtaining an aimed product.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06339045B1 |
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| Source dataset | uspto-grants-2002_01 |
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| ORD ID | ord-4e8cf4c5f1fb4848b7d607c7c9bd8232 |
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| Source note | uspto-grants-2002_01 |
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