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HRID 27148作成日:2026年10月25日

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

https://huagongshe.com/reaction/27148

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-p-chloroanilinoacetaldehyde diethyl acetalHCID 20460579—
溶媒WaterHCID 962—
生成物1-(N-benzyloxycarbonyl-p-chloroanilinomethyl)-6,7-dihydroxy-1,2,3,4-tetrahydroisoquinoline hydrochlorideHCID 20460510111.3%

反応手順

N-benzyloxycarbonyl-p-chloroanilinoacetaldehyde diethyl acetal (10 g) and 3,4-dihydroxyphenethylamine hydrochloride (4.2 g) were added to a mixture of n-butyl alcohol (100 ml) and water (14 ml) and then the mixture was refluxed for 4 hours. The above-mentioned acetal (1 g) was added to the mixture and the resultant mixture was refluxed for 4 hours. The reaction mixture was concentrated to dryness under reduced pressure and the residue was washed with ethyl acetate and collected by filtration. The crystals were recrystallized from a mixture of methanol and ether to give 1-(N-benzyloxycarbonyl-p-chloroanilinomethyl)-6,7-dihydroxy-1,2,3,4-tetrahydroisoquinoline hydrochloride (7.0 g), mp 210° to 212° 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-29324dd202c84c9b9e0a37545ed7a11b
出典メモuspto-grants-1980_09