戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 27151作成日:2026年10月24日

1-Butanol → 1-(N-benzyloxycarbonyl-m-fluoroanilinomethyl)-6,7-dihydroxy-1,2,3,4-tetrahydroisoquinoline hydrochloride

https://huagongshe.com/ja/reaction/27151

反応式

関与物質

役割名称HCID仕込み量
反応物1-ButanolHCID 263—
反応物Dopamine HydrochlorideHCID 65340—
反応物N-benzyloxycarbonyl-m-fluoroanilinoacetaldehyde diethyl acetalHCID 20460585—
溶媒WaterHCID 962—
生成物1-(N-benzyloxycarbonyl-m-fluoroanilinomethyl)-6,7-dihydroxy-1,2,3,4-tetrahydroisoquinoline hydrochlorideHCID 2046054981%

反応手順

N-benzyloxycarbonyl-m-fluoroanilinoacetaldehyde diethyl acetal (15 g) and 3,4-dihydroxyphenethylamine hydrochloride (5.75 g) were added to a mixture of n-butyl alcohol (150 ml) and water (20 ml) and then the mixture was refluxed for 11 hours in a stream of nitrogen. The reaction mixture was concentrated to dryness and the residue was in turn washed with ether and with a mixture of ether: ethyl acetate (2:1) and then crystallized with acetone. The crystals were collected by filtration to give 1-(N-benzyloxycarbonyl-m-fluoroanilinomethyl)-6,7-dihydroxy-1,2,3,4-tetrahydroisoquinoline hydrochloride (11.27 g), mp 184° to 186° C. (dec).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04220647
出典データセットuspto-grants-1980_09
ORD IDord-3721dd1e793345b5afbf9545d29a7c99
出典メモuspto-grants-1980_09