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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 19557생성일: 2026년 10월 24일

Pyridine → 1-hydroxyimino-6-(2-morpholine-4-yl-ethoxy)-3-pheny-1H-indene-2-carboxylic acid cyclohexylamide

https://huagongshe.com/ko/reaction/19557

반응식

참여 물질

역할이름HCID투입량
반응물PyridineHCID 1049—
반응물Hydroxyamine hydrochlorideHCID 443297—
반응물6-(2-morpholine-4-ylethoxy)-1-oxo-3-pheny-1H-indene-2-carboxylic acid cyclohexylamideHCID 68698349—
용매EthanolHCID 702—
생성물1-hydroxyimino-6-(2-morpholine-4-yl-ethoxy)-3-pheny-1H-indene-2-carboxylic acid cyclohexylamideHCID 8661531464.1%

반응 단계

6-(2-Morpholine-4-ylethoxy)-1-oxo-3-phenyl-1H-indene-2-carboxylic acid cyclohexylamide (130 mg, 0.28%) obtained in Step 4 was dissolved in ethanol (20 mL), and hydroxylamine hydrochloride (60 mg, 0.85 mmol) and pyridine (892 mg, 1.13 mmol) were added thereto. The mixture was refluxed for 1 hr, and cooled to RT, and extracted with dichloromethane. The organic layer was separated, dried over anhydrous MgSO4 and concentrated under a reduced pressure. The resulting residue was purified by flash chromatography to obtain 86 mg of 1-hydroxyimino-6-(2-morpholine-4-yl-ethoxy)-3-phenyl-1H-indene-2-carboxylic acid cyclohexylamide (yield: 64%). Subsequently, 1-hydroxyimino-6-(2-morpholine-4-yl-ethoxy)-3-phenyl-1H-indene-2-carboxylic acid cyclohexylamide (80 mg, 0.17 mmol) thus obtained was dissolved in methanol (20 mL) and 10%-palladium (100 mg) was added thereto. The mixture was stirred for 15 hrs at RT while providing H2 gas thereto using a balloon, filtered through celite, and concentrated under a reduced pressure. Then, the resulting residue was purified by flash chromatography to obtain 14 mg of the titled compound (yield: 18%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07745439B2
출처 데이터셋uspto-grants-2010_06
ORD IDord-fd7b1b84ee4b42b392ba7009b775e8b3
출처 메모uspto-grants-2010_06