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HRID 981173作成日:2026年10月26日

Diketene → FR 76830

https://huagongshe.com/reaction/981173

反応式

関与物質

役割名称HCID仕込み量
反応物DiketeneHCID 12661—
反応物3-NitrochalconeHCID 94862—
反応物2-MorpholinoethylamineHCID 408285—
反応物Ammonium AcetateHCID 517165—
反応物N-(2-morpholin-4-ylethyl)-3-oxobutanamideHCID 4076516—
溶媒Methyl Isobutyl KetoneHCID 7909—
生成物FR 76830HCID 308265739.6%

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04990507
出典データセットuspto-grants-1991_02
ORD IDord-c4c7330502bf48cb83081acf5eead5c0
出典メモuspto-grants-1991_02