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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 481137생성일: 2026년 10월 26일

Ethyl N-(2,3-dichloro-6-nitrobenzyl)glycine → ethyl-N-(6-amino-2,3-dichlorobenzyl)glycine

https://huagongshe.com/reaction/481137

반응식

참여 물질

역할이름HCID투입량
반응물Ethyl N-(2,3-dichloro-6-nitrobenzyl)glycineHCID 22439334—
촉매PlatinumHCID 23939—
생성물ethyl-N-(6-amino-2,3-dichlorobenzyl)glycineHCID 67080112—

반응 단계

Ethyl N-(2,3-dichloro-6-nitrobenzyl)glycine (compound VI) may also be catalytically hydrogenated using a sulfided platinum on carbon catalyst under hydrogen pressure. The catalyst is then removed by filtration and the filtrate concentrated, diluted with water and an organic solvent and basified using an alkali to a pH of about 9-10. The organic phase is separated and concentrated and the crude material purified by low temperature recrystallization to give ethyl-(6-amino-2,3-dichlorobenzyl)glycine (compound I). 6,7-dichloro-1,5-dihydroimidazo[2,1-b]quinazoline-2(3H)one (compound III) may be prepared from compound II by suspending 5,6-dichloro-3,4-dihydro-2(1H)iminoquinazoline-3-acetate HBR (compound II) in water and adding an organic base such as TEA. After filtering the solution the filtered cake is washed in water and the solids suspended in alcohol. After filtering, the solids are rinsed in an alcohol and dried to give compound III.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06653500B2
출처 데이터셋uspto-grants-2003_11
ORD IDord-13078e11f0c1437fae99de3ec5765b6e
출처 메모uspto-grants-2003_11