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HRID 1777063作成日:2026年10月25日

3-Chloro-6-hydroxyacetophenone → N-[(E)-1-(5-chloro-2-hydroxyphenyl)ethylideneamino]-4-morpholin-4-ylsulfonylbenzamide

https://huagongshe.com/reaction/1777063

反応式

関与物質

役割名称HCID仕込み量
反応物3-Chloro-6-hydroxyacetophenoneHCID 74061—
反応物4-(Morpholinosulfonyl)benzohydrazideHCID 864339—
溶媒Acetic AcidHCID 176—
溶媒MethanolHCID 887—
生成物N-[(E)-1-(5-chloro-2-hydroxyphenyl)ethylideneamino]-4-morpholin-4-ylsulfonylbenzamideHCID 13637436250.6%

反応条件

温度120 °C

反応手順

4-(morpholinosulfonyl)benzohydrazide (100 mg, 0.350 mmol) and 1-(5-chloro-2-hydroxyphenyl)ethanone (59.8 mg, 0.350 mmol) was dissolved in methanol (Volume: 4 ml) in the presence of acetic acid as a catalyst and then the reaction mixture was heated via microwave irradiation to 120° C. for 30 min. Reaction was monitored by TLC. After completion of the reaction, following cooling, the solvent was removed by vacuum and the resulting crude material was purified by flash column chromatography (2% CH3OH/CH2Cl2) afforded the product (E)-N′-(1-(5-chloro-2-hydroxyphenyl)ethylidene)-4-(morpholinosulfonyl)benzohydrazide (80 mg, 0.177 mmol, 50.6% yield) as a solid. 1H NMR (DMSO-d6, 400 MHz): δ 8.16 (m, 2H), 7.89 (m, 2H), 7.67 (d, 1H, J=2.4 Hz), 7.35 (dd, 1H, J=2.4 & 8.8 Hz), 6.95 (d, 1H, J=8.4 Hz), 3.64 (m, 4H), 2.92 (m, 4H), 2.49 (s, 3H). Mass [M+H]+: 438.0

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09266838B2
出典データセットuspto-grants-2016_02
ORD IDord-8317aba7720c4775a9f682e8f963fd36
出典メモuspto-grants-2016_02