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HRID 2183708作成日:2026年10月27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/reaction/2183708

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US06900220B2
出典データセットuspto-grants-2005_05
ORD IDord-10b30f30a6b34483809b31f83eb5d43d
出典メモuspto-grants-2005_05