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HRID 1596537作成日:2026年10月26日

4-Acetamidobenzenesulfonyl azide → Benzyl 5-diazo-1-(3,4-dichlorobenzyl)-4-oxo-4,5,6,7-tetrahydroindole-2-carboxylate

https://huagongshe.com/reaction/1596537

反応式

関与物質

役割名称HCID仕込み量
反応物4-Acetamidobenzenesulfonyl azideHCID 5129185—
反応物Benzyl 1-(3,4-dichlorobenzyl)-5-formyl-4-oxo-4,5,6,7-tetrahydroindole-2-carboxylateHCID 9846845—
溶媒TriethylamineHCID 8471—
生成物Benzyl 5-diazo-1-(3,4-dichlorobenzyl)-4-oxo-4,5,6,7-tetrahydroindole-2-carboxylateHCID 2170218762.3%

反応手順

Triethyl amine (0.36 mL) was added dropwise to a solution of benzyl 1-(3,4-dichlorobenzyl)-5-formyl-4-oxo-4,5,6,7-tetrahydroindole-2-carboxylate (0.5 g) and p-acetamidobenzenesulphonyl azide (305 mg) at room temperature, and stirred for 18 hours to give a brown solution. The solvent was removed in vacuo to afford a brown oil. Purification by column chromatography, using iso-hexane : 20% ethyl acetate as eluent afforded the title compound as a pale yellow solid (0.31 g, 62%), NMR d(CDCl3) 2.80 (2H, t), 3.05 (2H, t), 5.13 (2H, s), 5.57 (2H, s), 6.76 (1H, dd), 7.05 (1H, s), 7.20-7.40 (7H, m); M/z (+) 456, 454 (M+).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06291507B1
出典データセットuspto-grants-2001_09
ORD IDord-284bc519df334634806c4a3f05accb08
出典メモuspto-grants-2001_09