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HRID 27147作成日:2026年10月24日

1-Butanol → 1-(N-benzyloxycarbonyl-3,4,5-trimethoxyanilinomethyl)-6,7-dihydroxy-1,2,3,4-tetrahydroisoquinoline hydrochloride

https://huagongshe.com/ja/reaction/27147

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-3,4,5-trimethoxyanilinoacetaldehyde diethyl acetalHCID 20460529—
溶媒WaterHCID 962—
生成物1-(N-benzyloxycarbonyl-3,4,5-trimethoxyanilinomethyl)-6,7-dihydroxy-1,2,3,4-tetrahydroisoquinoline hydrochlorideHCID 2046055170.1%

反応手順

N-benzyloxycarbonyl-3,4,5-trimethoxyanilinoacetaldehyde diethyl acetal (21 g) and 3,4-dihydroxyphenethylamine hydrochloride (8.3 g) were added to a mixture of n-butyl alcohol (210 ml) and water (30 ml) and then the mixture was refluxed for 11 hours in a stream of nitrogen. In the course of the reaction, amounts of the above-mentioned acetal (2.1 g, 2.1 g and 4.2 g) were added to the mixture after 5 hours, 6 hours and 7 hours, respectively, from the beginning of the reaction, respectively. The reaction mixture was concentrated to dryness under reduced pressure and the residue was washed with ether and acetone to give 1-(N-benzyloxycarbonyl-3,4,5-trimethoxyanilinomethyl)-6,7-dihydroxy,1,2,3,4-tetrahydroisoquinoline hydrochloride (16.3 g). The product was recrystallized from a mixed solvent of ethanol and ether to give a pure product, mp 197° to 199° 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-a43635fea12b4c809e92f1044b1ffa83
出典メモuspto-grants-1980_09