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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 981173생성일: 2026년 10월 25일

Diketene → FR 76830

https://huagongshe.com/reaction/981173

반응식

참여 물질

역할이름HCID투입량
반응물DiketeneHCID 12661—
반응물3-NitrochalconeHCID 94862—
반응물2-MorpholinoethylamineHCID 408285—
반응물Ammonium AcetateHCID 517165—
반응물N-(2-morpholin-4-ylethyl)-3-oxobutanamideHCID 4076516—
용매Methyl Isobutyl KetoneHCID 7909—
생성물FR 76830HCID 308265739.6%

반응 단계

A solution of N-(2-aminoethyl)morpholine (170.5 g) in methyl isobutyl ketone (200 ml) was added portionwise to a solution of diketene (102 ml) in methyl isobutyl ketone (1.3 () at -30 to -10° C. under stirring and the mixture was stirred at -10 to 0° C. for one hour. To the resultant solution containing N-(2-morpholinoethyl)acetoacetamide, was added 3-(3-nitrophenyl)-1-phenyl-2-propen-1-one (220.4 g) and ammonium acetate (100 g) and the mixture was stirred at 80° C. for 4.5 hours. The reaction mixture was washed with water and dried over magnesium sulfate. To the filtrate containing 1,4-dihydro-3-(2-morpholinoethylcarbamoyl)-2-methyl-4-(3-nitrophenyl)-6-phenylpyridine was added manganese dioxide (700 g) and the resultant mixture was stirred at 80° C. for 2 hours. Manganese dioxide was filtered off and the filtrate was evaporated in vacuo. A mixture of ethyl acetate and water was added to the residue and adjusted to pH 1.0 with 10% hydrochloric acid. The separated aqueous layer was adjusted to pH 9.0 with 20% aqueous potassium carbonate and extracted with a mixture of ethyl acetate and tetrahydrofuran. The extract was washed with brine and dried over magnesium sulfate. The solvent was evaporated in vacuo and the residue was recrystallized from ethanol to give 3-(2-morpholinoethylcarbamoyl)-2-methyl-4-(3-nitrophenyl)-6-phenylpyrid ine (154 g, yield 39.6 %), which was identified as the compound of Examples 9-(20 and 24-(3) by their physical data.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04990507
출처 데이터셋uspto-grants-1991_02
ORD IDord-c4c7330502bf48cb83081acf5eead5c0
출처 메모uspto-grants-1991_02