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HRID 35249作成日:2026年10月24日

Diethylamine → N,N-diethyl-4-(1-methyl-1,2,3,4-tetrazol-5-yl)thio-butyramide

https://huagongshe.com/ja/reaction/35249

反応式

関与物質

役割名称HCID仕込み量
反応物DiethylamineHCID 8021—
反応物TriethylamineHCID 8471—
反応物Isobutyl chloroformateHCID 62365—
反応物HCID 178482013HCID 178482013—
溶媒TetrahydrofuranHCID 8028—
生成物N,N-diethyl-4-(1-methyl-1,2,3,4-tetrazol-5-yl)thio-butyramideHCID 2115394854%

反応手順

4-(1-Methyl-1,2,3,4-tetrazol-5-yl)thio-butyric acid (2 g) is dissolved in dry tetrahydrofuran (30 ml), and thereto is added triethylamine (1.1 g). To the mixture is added dropwise with stirring isobutyl chloroformate (1.5 g) under ice-cooling. The mixture is stirred at room temperature for 30 minutes. To the mixture is further added dropwise with stirring diethylamine (0.9 g) at room temperature, and the mixture is stirred for 2 hours. The mixture is concentrated under reduced pressure, and the resulting residue is purified by subjecting it to column chromatography (Kieselgel 60, made by Merck & Co.). By eluting with n-hexaneethyl acetate (1:1), there is obtained N,N-diethyl-4-(1-methyl-1,2,3,4-tetrazol-5-yl)thio-butyramide (1.4 g), colorless liquid, nD17.5 =1.5227.

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-78fb2885d3ea475e8b0b26aab8d14d29
出典メモuspto-grants-1988_08