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HRID 234822作成日:2026年10月25日

Methylhydrazine → 2-methyl-5-(p-toluenesulfonyloxy)isoquino [8,7,6-cd]indazole-6(2H)-one

https://huagongshe.com/reaction/234822

反応式

関与物質

役割名称HCID仕込み量
反応物MethylhydrazineHCID 6061—
反応物9-Fluoro-6-(p-toluenesulfonyloxy)benzo[g]isoquinoline-5,10-dioneHCID 10572880—
反応物9-Chloro-6-(p-toluenesulfonyloxy)benzo[g]isoquinoline-5,10-dioneHCID 19974754—
溶媒PyridineHCID 1049—
生成物2-methyl-5-(p-toluenesulfonyloxy)isoquino [8,7,6-cd]indazole-6(2H)-oneHCID 15337874—

反応手順

The 1:1 mixture of 9-fluoro-6-(p-toluenesulfonyloxy)benzo[g]isoquinoline-5,10-dione and 9-chloro-6-(p-toluenesulfonyloxy)benzo[g]isoquino line-5,10-dione, of Preparative Example 15a, (0.041 g) is dissolved in dry pyridine (2 mL) and a freshly prepared 1M solution of N-methyhydrazine in pyridine (0.183 mL) is added. After stirring for three hours at room temperature the reaction mixture is concentrated to dryness and added with water (5 mL), with NaH2PO4 saturated solution (5 mL) and extracted several times with methylene chloride (50 mL). The combined organic solutions are dried ever anhydrous sodium sulfate and the solvent is removed at reduced pressure. The obtained residue is purified by silica-gel column chromatography (eluant: methylene chloride/ethyl acetate 90/10 v/v (50 mL), then 75/25 (50 mL), then 60/40 (50 mL) and finally 40/60 (50 mL) to give 2-methyl-5-(p-toluenesulfonyloxy)isoquino[8,7,6-cd]indazole-6(2H)-one.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05596097
出典データセットuspto-grants-1997_01
ORD IDord-1ab01fa438ec4a2eb259307d9c283e7f
出典メモuspto-grants-1997_01