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HRID 427342作成日:2026年10月24日

Triethylamine → Diisopropylether ethyl acetate

https://huagongshe.com/ja/reaction/427342

反応式

関与物質

役割名称HCID仕込み量
反応物TriethylamineHCID 8471—
反応物Thionyl ChlorideHCID 24386—
反応物4-(Morpholine-4-carbonyl)anilineHCID 577815—
反応物5-Methoxy-8-nitro-1,2,3,4-tetrahydronaphthalene-2-carboxylic acidHCID 18622509—
触媒DimethylformamideHCID 6228—
溶媒WaterHCID 962—
溶媒TolueneHCID 1140—
溶媒DichloromethaneHCID 6344—
生成物N-(4-Morpholinocarbonylphenyl)-5-methoxy-8-nitro-1,2,3,4-tetrahydronaphthalene-2-carboxamideHCID 18622500—
生成物Diisopropylether ethyl acetateHCID 22281796315.3%

反応条件

温度60 °C

反応手順

A mixture of 5-methoxy-8-nitro-1,2,3,4-tetrahydronaphthalene-2-carboxylic acid (1.0 g, 4 mmol), toluene (20 mL), N,N-dimethylformamide (10 drops) and thionyl chloride (1.5 mL, 20 mmol) was heated at 60° C. for 1 h. The solvents were removed in vacuo and the residue, dissolved in methylene chloride (20 mL), was added to a solution of 4-aminobenzoylmorpholine (820 mg, 4 mmol, described in: Deylin J. P. J. Chem. Soc. Perkin Trans I, 1975, 830-841) and triethylamine (800 mg, 8 mmol) in methylene chloride (30 mL) at 5° C. After stirring at 20° C. for 2 h, water was added and the organic phase was separated, dried and the solvent removed in vacuo. The oily residue was crystallized from diisopropyl ether/ethyl acetate affording 1.2 g (73% yield) of the title compound as crystals: mp 186-189° C.; EIMS (70 eV) m/z (relative intensity) 439 (20, M+).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06313118B1
出典データセットuspto-grants-2001_11
ORD IDord-717ba65c41b6443da0555ea0645bbe72
出典メモuspto-grants-2001_11