Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Triphenyl phosphite | HCID 7540 | — |
| Edukt | 2-Amino-3-methoxybenzoic acid | HCID 255720 | — |
| Edukt | beta-Alanine, ethyl ester, hydrochloride | HCID 458475 | — |
| Edukt | 2,2-Difluoro-2-(5-fluoropyridin-2-yl)acetic acid | HCID 66609553 | — |
| Lösungsmittel | Pyridine | HCID 1049 | — |
| Produkt | HCID 178488826 | HCID 178488826 | 71% |
Reaktionsschritte
To 2,2-difluoro-2-(5-fluoropyridin-2-yl)acetic acid from Example 33 step A (1 g, 5.23 mmol) and 2-amino-3-methoxybenzoic acid (875 mg, 5.23 mmol) in pyridine (15 mL) was added triphenyl phosphite (1.51 mL, 5.75 mmol) and the mixture was heated in a microwave synthesizer at 150° C. for 10 min. The mixture was allowed to cool to rt and then ethyl 3-aminopropanoate hydrochloride (883 mg, 5.75 mmol) was added. The mixture was heated in a microwave synthesizer at 190° C. for 4 min and then concentrated under reduced pressure. THF (10 mL) and sodium ethoxide (21% in EtOH, 4 mL) were added, and the mixture was stirred at 60° C. for 0.5 h. The mixture was allowed to cool and concentrated under reduced pressure. The residue was dissolved in water and the pH was adjusted to <4 by addition of 4 N HCl. The precipitate was collected by filtration, washed with water, and dried on the funnel to afford 2-(difluoro(5-fluoropyridin-2-yl)methyl)-8-methoxyquinazolin-4-ol (1.19 g, 71%). LC-MS (ESI) m/z 322 (M+H)+.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US08633207B2 |
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| Quelldatensatz | uspto-grants-2014_01 |
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| ORD ID | ord-f15bdac829d74917a33560b0fcef7c35 |
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| Quellennotiz | uspto-grants-2014_01 |
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