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HRID 8721Erstellt: 24. Oktober 2026
Diisopropylethylamine → 2-(1-benzyl-1,4,6,7-tetrahydro-imidazo[4,5-c]pyridin-5-yl)-6,7-dimethoxy-3H-quinazolin-4-one
https://huagongshe.com/de/reaction/8721
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | Diisopropylethylamine | HCID 81531 | — |
| Edukt | 1-Benzyl-1,4,6,7-tetrahydro-imidazo[4,5-c]pyridine dihydrochloride | HCID 21983657 | — |
| Edukt | 2-Chloro-6,7-dimethoxy-3H-quinazolin-4-one | HCID 135456664 | — |
| Lösungsmittel | Water | HCID 962 | — |
| Lösungsmittel | 2-Methoxyethanol | HCID 8019 | — |
| Produkt | 2-(1-benzyl-1,4,6,7-tetrahydro-imidazo[4,5-c]pyridin-5-yl)-6,7-dimethoxy-3H-quinazolin-4-one | HCID 135723508 | 29,9% |
Reaktionsschritte
A mixture of 2-chloro-6,7-dimethoxy-3H-quinazolin-4-one 1 (wherein R is methyl and Z is —C(O)—, 296 mg, 1.24 mmol), 1-benzyl-1,4,6,7-tetrahydro-imidazo[4,5-c]pyridine dihydrochloride 15a (440 mg, 1.54 mmol)) and diisopropylethylamine (1.2 g, 9.26 mmol) in 2-methoxyethanol (10 mL) was stirred at 120° C. for 6 hours. The reaction mixture was concentrated in vacuo to give an oil residue, which was diluted with water. The white precipitate that formed was collected by filtration to give 155 mg of 2-(1-benzyl-1,4,6,7-tetrahydro-imidazo[4,5-c]pyridin-5-yl)-6,7-dimethoxy-3H-quinazolin-4-one 501, [M+H]+=418.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US07091200B2 |
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| Quelldatensatz | uspto-grants-2006_08 |
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| ORD ID | ord-1072292ad8ec44c99727818e337ae56f |
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| Quellennotiz | uspto-grants-2006_08 |
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