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HRID 8724作成日:2026年10月24日

Ethanol → 6,7-dimethoxy-2-(1-m-tolyl-1,4,6,7-tetrahydro-imidazo[4,5-c]pyridin-5-yl)-3H-quinazolin-4-one

https://huagongshe.com/ja/reaction/8724

反応式

関与物質

役割名称HCID仕込み量
反応物EthanolHCID 702—
反応物TriethylamineHCID 8471—
反応物1-m-tolyl-4,5,6,7-tetrahydro-1H-imidazo[4,5-c]pyridineHCID 21983644—
反応物2-Chloro-6,7-dimethoxy-3H-quinazolin-4-oneHCID 135456664—
溶媒1-MethoxyethanolHCID 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-oneHCID 13553251656.9%

反応条件

温度100 °C

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

DOI10.6084/m9.figshare.5104873.v1
特許番号US07091200B2
出典データセットuspto-grants-2006_08
ORD IDord-2c8bf22c88d141f18e9c170291be32b9
出典メモuspto-grants-2006_08