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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 234827생성일: 2026년 10월 26일

2-Hydrazinyl-N,N-dimethylethanamine → 5-chloro-2-[2-(dimethylamino)ethyl]-10-(p-methoxybenzyloxy) isoquino[5,6,7-cd]indazole-6(2H)-one

https://huagongshe.com/reaction/234827

반응식

참여 물질

역할이름HCID투입량
반응물2-Hydrazinyl-N,N-dimethylethanamineHCID 120552—
반응물9-Chloro-6-fluoro-4-(p-methoxy benzyloxy)benzo[g]isoquinoline-5,10-dioneHCID 15361940—
용매PyridineHCID 1049—
생성물5-chloro-2-[2-(dimethylamino)ethyl]-10-(p-methoxybenzyloxy) isoquino[5,6,7-cd]indazole-6(2H)-oneHCID 10647769—

반응 단계

A solution of N-[2-(dimethylamino)ethyl]hydrazine (8.5 mg) in pyridine (0.5 mL) is added to 9-chloro-6-fluoro-4-(p-methoxybenzyloxy) benzo[g]isoquinoline-5,10-dione of Preparative Example 29 (13 mg) over a period of 2 minutes at 0° C. under a nitrogen blanket and the mixture is stirred for 2 h. The excess pyridine and some excess hydrazine are removed under a nitrogen stream. The residue is placed under vacuum overnight. The product is purified by thick layer chromathography (silica gel, 10 cm by 20 cm) using 4% methanol/96% dicloromethane. The major yellow band is scraped from the plate and the yellow compound extracted into 25% methanol/75% dicloromethane. Removal of the solvent gives 5-chloro-2-[2-(dimethylamino)ethyl]-10-(p-methoxybenzyloxy) isoquino[5,6,7-cd]indazole-6(2H)-one (3 mg) as an amorphous solid.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05596097
출처 데이터셋uspto-grants-1997_01
ORD IDord-32bfe993475a41df8acf5a5c914ae87b
출처 메모uspto-grants-1997_01