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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 419282생성일: 2026년 10월 26일

Hydroxylamine → Benzyloxy-3-nitro[1,5]naphthyridin-4-amine

https://huagongshe.com/reaction/419282

반응식

참여 물질

역할이름HCID투입량
반응물HydroxylamineHCID 787—
반응물Benzyloxy-4-chloro-3-nitroquinolineHCID 21075762—
반응물Benzyloxy-4-chloro-3-nitro[1,5]naphthyridineHCID 66650176—
생성물Benzyloxy-3-nitro[1,5]naphthyridin-4-amineHCID 66649873—
생성물Benzyloxy-3-nitroquinolin-4-amineHCID 66649911—

반응 단계

In step (5) of Reaction Scheme I, a benzyloxy-4-chloro-3-nitroquinoline or benzyloxy-4-chloro-3-nitro[1,5]naphthyridine of Formula XIX is treated with an amino alcohol of formula HO—(CH2)c—CH2—NH2 to provide a benzyloxy-3-nitroquinolin-4-amine or benzyloxy-3-nitro[1,5]naphthyridin-4-amine of Formula XX. The reaction is conveniently carried out by adding the amino alcohol of formula HO—(CH2)c—CH2—NH2 to a solution of a compound of Formula XIX in a suitable solvent such as dichloromethane in the presence of a tertiary amine such as triethylamine. The reaction can be carried out at ambient temperature or at an elevated temperature such as, for example, the reflux temperature of the solvent. The reaction product can be isolated using conventional methods.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08093390B2
출처 데이터셋uspto-grants-2012_01
ORD IDord-8e73153255434929bf0f88c1d544d9d9
출처 메모uspto-grants-2012_01