関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Ethanol | HCID 702 | — |
| 反応物 | Triethylamine | HCID 8471 | — |
| 反応物 | 1-m-tolyl-4,5,6,7-tetrahydro-1H-imidazo[4,5-c]pyridine | HCID 21983644 | — |
| 反応物 | 2-Chloro-6,7-dimethoxy-3H-quinazolin-4-one | HCID 135456664 | — |
| 溶媒 | 1-Methoxyethanol | HCID 3015637 | — |
| 生成物 | 6,7-dimethoxy-2-(1-m-tolyl-1,4,6,7-tetrahydro-imidazo[4,5-c]pyridin-5-yl)-3H-quinazolin-4-one | HCID 135532516 | 56.9% |
反応手順
A mixture of 1-m-tolyl-4,5,6,7-tetrahydro-1H-imidazo[4,5-c]pyridine 18a (100 mg, 0.5 mmol), 2-chloro-6,7-dimethoxy-3H-quinazolin-4-one 1b (100 mg, 0.4 mmol), and triethylamine (140 μL, 1.0 mmol) in 10 mL methoxyethanol was heated at 100° C. under nitrogen for 12 hr. The mixture was pumped to constant weight. The resulting residue was slurried with hot ethanol and allowed to reach ambient temperature. Vacuum filtration provided 95 mg of 6,7-dimethoxy-2-(1-m-tolyl-1,4,6,7-tetrahydro-imidazo[4,5-c]pyridin-5-yl)-3H-quinazolin-4-one, 601, [M+H]+=418, as a white solid.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US07091200B2 |
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| 出典データセット | uspto-grants-2006_08 |
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| ORD ID | ord-2c8bf22c88d141f18e9c170291be32b9 |
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| 出典メモ | uspto-grants-2006_08 |
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