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HRID 234822생성일: 2026년 10월 26일

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

https://huagongshe.com/reaction/234822

반응식

참여 물질

역할이름HCID투입량
반응물MethylhydrazineHCID 6061—
반응물9-Fluoro-6-(p-toluenesulfonyloxy)benzo[g]isoquinoline-5,10-dioneHCID 10572880—
반응물9-Chloro-6-(p-toluenesulfonyloxy)benzo[g]isoquinoline-5,10-dioneHCID 19974754—
용매PyridineHCID 1049—
생성물2-methyl-5-(p-toluenesulfonyloxy)isoquino [8,7,6-cd]indazole-6(2H)-oneHCID 15337874—

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05596097
출처 데이터셋uspto-grants-1997_01
ORD IDord-1ab01fa438ec4a2eb259307d9c283e7f
출처 메모uspto-grants-1997_01