関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | 5-Amino-1,2,3,4-tetrahydroisoquinoline | HCID 16217499 | — |
| 反応物 | 2-Chloro-6,7-dimethoxy-3H-quinazolin-4-one | HCID 135456664 | — |
| 溶媒 | 1-Methoxyethanol | HCID 3015637 | — |
| 生成物 | 2-(5-amino-3,4-dihydro-1H-isoquinolin-2-yl)-6,7-dimethoxy-3H-quinazolin-4-one | HCID 136347701 | 49.7% |
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
| 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-ceeddba39e0c466fa26fb10a6049ce5d |
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| 出典メモ | uspto-grants-2006_08 |
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