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HRID 65067作成日:2026年10月24日

Carbon Disulfide → n-Hexyl (3S)-3-hydroxymethyl-1,2,3,4-tetrahydro-beta-carboline-2-carbodithioate

https://huagongshe.com/ja/reaction/65067

反応式

関与物質

役割名称HCID仕込み量
反応物Carbon DisulfideHCID 6348—
反応物1-BromohexaneHCID 8101—
反応物TriethylamineHCID 8471—
反応物(3S)-3-hydroxymethyl-1,2,3,4-tetrahydro-beta-carbolineHCID 13375506—
溶媒Dimethyl SulfoxideHCID 679—
生成物n-Hexyl (3S)-3-hydroxymethyl-1,2,3,4-tetrahydro-beta-carboline-2-carbodithioateHCID 1339298173.2%

反応手順

(3S)-3-Hydroxymethyl-1,2,3,4-tetrahydro-β-carboline (2.02 g) is dissolved in dimethylsulfoxide (10 ml), and thereto are added triethylamine (1.67 ml) and CS2 (0.72 ml), and the mixture is stirred at room temperature for 20 minutes. To the reaction mixture is added dropwise n-hexyl bromide (1.98 g), and the mixture is stirred at room temperature for 2.5 hours. The reaction mixture is poured onto ice-water and the mixture is extracted with ethyl acetate. The ethyl acetate layer is washed with water, dried over sodium sulfate, and then distilled to remove the solvent. The residue is recrystallized from ether-n-hexane to give the title compound (2.65 g, 73.2%) as colorless needles, m.p. 102°-106° C. NMR (CDCl3, δ): 0.90 (broad, t, 3H, --(CH2)5 --CH3); Mass m/e: 362 (M+), 244 (M+ --C6H13SH); [α]D20 +130.0° (c=1.0, methanol).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04612317
出典データセットuspto-grants-1986_09
ORD IDord-537bca8a081e45dbbc8a50af57fc05e0
出典メモuspto-grants-1986_09