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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 540802생성일: 2026년 10월 24일

Ammonium Hydroxide → Oxane-4-carboxamide

https://huagongshe.com/ko/reaction/540802

반응식

참여 물질

역할이름HCID투입량
반응물Ammonium HydroxideHCID 14923—
반응물2H-Pyran-4-carboxylic acid, tetrahydro-, methyl esterHCID 2773520—
반응물Benzyloxy-4-chloro-3-nitroquinolineHCID 21075762—
반응물Benzyloxy-3-nitroquinolin-4-amineHCID 66649911—
용매MethanolHCID 887—
용매DichloromethaneHCID 6344—
용매TriethylamineHCID 8471—
생성물Oxane-4-carboxamideHCID 13197203—

반응 단계

In step (5) of Reaction Scheme I, a benzyloxy-4-chloro-3-nitroquinoline of Formula XIX is treated with an amine of Formula R1—NH2 to provide a benzyloxy-3-nitroquinolin-4-amine of Formula XX. The reaction is conveniently carried out by adding the amine of Formula R1—NH2 to a solution of the benzyloxy-4-chloro-3-nitroquinoline of Formula XIX in a suitable solvent such as dichloromethane or methanol 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. Several mines of Formula R1—NH2 are commercially available; others can be prepared by known synthetic methods. For example, methyl tetrahydro-2H-pyran-4-carboxylate treated with ammonium hydroxide to form tetrahydro-2H-pyran-4-carboxamide, which can then be reduced with lithium aluminum hydride to provide tetrahydro-2H-pyran-4-ylmethylamine.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08871782B2
출처 데이터셋uspto-grants-2014_10
ORD IDord-ce9fce475629448ab676fa3dcd87db44
출처 메모uspto-grants-2014_10