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HRID 35250作成日:2026年10月23日

Homoveratrylamine → N-[2-(3,4-dimethoxyphenyl)ethyl]-4-(1-methyl-1,2,3,4-tetrazol-5-yl)thio-butyramide

https://huagongshe.com/ja/reaction/35250

反応式

関与物質

役割名称HCID仕込み量
反応物HomoveratrylamineHCID 8421—
反応物Isobutyl chloroformateHCID 62365—
反応物1,8-Diazabicyclo(5.4.0)undec-7-eneHCID 81184—
反応物HCID 178482013HCID 178482013—
溶媒TetrahydrofuranHCID 8028—
生成物N-[2-(3,4-dimethoxyphenyl)ethyl]-4-(1-methyl-1,2,3,4-tetrazol-5-yl)thio-butyramideHCID 5405021841%

反応手順

4-(1-Methyl-1,2,3,4-tetrazol-5-yl)thio-butyric acid (45 mmole) is dissolved in tetrahydrofuran (50 ml), and thereto is added DBU (50 mmole). To the mixture is added dropwise with stirring isobutyl chloroformate (50 mmole) under ice-cooling and the mixture is stirred at room temperature for 30 minutes. To the mixture is added dropwise 2-(3,4-dimethoxyphenyl)ethylamine (54 mmole) and the mixture is further stirred at room temperature for 2 hours. After the solvent is distilled off under reduced pressure, the resulting residue is extracted with chloroform. The chloroform layer is washed with 5% aqueous hydrochloric acid, an aqueous saturated sodium hydrogen carbonate solution and an aqueous saturated sodium chloride solution and dried over anhydrous sodium sulfate. After distilling off chloroform, the residue is subjected to column chromatography (Wakogel C-200, eluting agent, chloroform) to isolate N-[2-(3,4-dimethoxyphenyl)ethyl]-4-(1-methyl-1,2,3,4-tetrazol-5-yl)thio-butyramide (yield: 41%) which is recrystallized from hexane-chloroform, colorless flaks, m.p. 70.5°-71.5° C.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04766120
出典データセットuspto-grants-1988_08
ORD IDord-4a703fea81f6423fa60176b3220e22fe
出典メモuspto-grants-1988_08