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HRID 1249037作成日:2026年10月26日

Ethanol → (3R)-2-[(Benzylthio)thiocarbonyl]-1,2,3,4-tetrahydro-beta-carboline-3-carboxylic acid

https://huagongshe.com/reaction/1249037

反応式

関与物質

役割名称HCID仕込み量
反応物EthanolHCID 702—
反応物Carbon DisulfideHCID 6348—
反応物Benzyl BromideHCID 7498—
反応物Sodium HydroxideHCID 14798—
反応物D-1,2,3,4-Tetrahydronorharman-3-carboxylic acidHCID 675102—
生成物(3R)-2-[(Benzylthio)thiocarbonyl]-1,2,3,4-tetrahydro-beta-carboline-3-carboxylic acidHCID 13561931—

反応手順

To a mixture of (3R)-1,2,3,4-tetrahydro-β-carboline-3-carboxylic acid (5.4 g), 2N NaOH (25 ml) and 50% ethanol (70 ml) is added dropwise carbon disulfide (1.5 ml) at room temperature. The mixture is stirred at room temperature for 30 minutes, and thereto is added dropwise benzyl bromide (3.5 ml), and the mixture is further stirred at the same temperature for 3 hours and then distilled to remover the solvent. To the residue is added water, and the mixture is extracted with ether. The aqueous layer is acidified with 10% HCl, extracted with ethyl acetate. The extract is washed with water, dried and distilled to remove the solvent. The residue is purified by silica gel column chromatography (solvent, chloroform:methanol=20:1) to give the title compound (4.5 g) as pale yellow powder.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04628057
出典データセットuspto-grants-1986_12
ORD IDord-0271a25bd06d4969a382bfb50786e4d6
出典メモuspto-grants-1986_12