Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Pyridine | HCID 1049 | — |
| Edukt | Thionyl Chloride | HCID 24386 | — |
| Edukt | HCID 964395 | HCID 964395 | — |
| Edukt | 7-Amino-quinoline-3-carboxylic acid (di-pyridin-2-yl-methyl)-amide | HCID 86585940 | — |
| Katalysator | Dimethylformamide | HCID 6228 | — |
| Lösungsmittel | Chloroform | HCID 6212 | — |
| Produkt | HCID 86585942 | HCID 86585942 | 34% |
Reaktionsschritte
A mixture of 2-benzyloxy-3-methoxybenzoic acid (109 mg, 0.42 mmol), thionyl chloride (5 ml) and 1 drop dimethylformamide was heated under reflux for 2 hr. The thionyl chloride was removed in vacuo, with traces being removed by adding methylene chloride and concentrating the solution in vacuo. The resulting 2-benzyloxy-3-methoxybenzoyl chloride was dissolved in chloroform and the solution was added dropwise to a solution of 7-amino-quinoline-3-carboxylic acid (di-pyridin-2-yl-methyl)-amide (75 mg, 0.21 mmol), 4-(N,N-dimethylaminopyridine) (DIMAP) (3 mg, 0.02 mmol) and pyridine (0.068 ml, 0.84 mmol) in chloroform at room temperature. The resulting solution was heated under reflux for 3 hr, then cooled to room temperature and concentrated to dryness in vacuo. The residue was dissolved in ethyl acetate, washed sequentially with water and brine, dried over anhydrous sodium sulfate and concentrated to dryness in vacuo. The residue (960 mg) was purified by column chromatography on silica gel, eluting with 98:2 chloroform/methanol to yield the title compound as a solid (40.3 mg, 34% yield).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US06713489B2 |
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| Quelldatensatz | uspto-grants-2004_03 |
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| ORD ID | ord-7c6d04060e1e4a2cb55986e17a5d12d7 |
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| Quellennotiz | uspto-grants-2004_03 |
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