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HRID 8730作成日:2026年10月23日

5-Amino-1,2,3,4-tetrahydroisoquinoline → 2-(5-amino-3,4-dihydro-1H-isoquinolin-2-yl)-6,7-dimethoxy-3H-quinazolin-4-one

https://huagongshe.com/ja/reaction/8730

反応式

関与物質

役割名称HCID仕込み量
反応物5-Amino-1,2,3,4-tetrahydroisoquinolineHCID 16217499—
反応物2-Chloro-6,7-dimethoxy-3H-quinazolin-4-oneHCID 135456664—
溶媒1-MethoxyethanolHCID 3015637—
生成物2-(5-amino-3,4-dihydro-1H-isoquinolin-2-yl)-6,7-dimethoxy-3H-quinazolin-4-oneHCID 13634770149.7%

反応条件

温度60 °C

反応手順

A mixture of 1,2,3,4-tetrahydro-isoquinolin-5-ylamine 24a (3.83 g, 25.84 mmol) and 2-chloro-6,7-dimethoxy-3H-quinazolin-4-one 1b (5.9 g, 24.54 mmol) in methoxyethanol (60 mL) was heated to 60° C. with stirring for 48 h. The volatiles were evaporated and the residue was purified by flash column chromatography eluting with 3% methanol in dichloromethane containing 0.3% of ammonium hydroxide to yield 4.3 g of 2-(5-amino-3,4-dihydro-1H-isoquinolin-2-yl)-6,7-dimethoxy-3H-quinazolin-4-one 110.

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-ceeddba39e0c466fa26fb10a6049ce5d
出典メモuspto-grants-2006_08