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HRID 395841作成日:2026年10月24日

Thionyl Chloride → 2-[[4-(4-Pyridyl)benzoyl]amino]-N-(4-methoxyphenyl)benzamide Hydrochloride

https://huagongshe.com/ja/reaction/395841

反応式

関与物質

役割名称HCID仕込み量
反応物Thionyl ChlorideHCID 24386—
反応物2-amino-N-(4-methoxyphenyl)benzamideHCID 478820—
反応物4-(Pyridin-4-yl)benzoic acidHCID 1520811—
溶媒PyridineHCID 1049—
溶媒TolueneHCID 1140—
生成物2-[[4-(4-Pyridyl)benzoyl]amino]-N-(4-methoxyphenyl)benzamide HydrochlorideHCID 1817443530.7%

反応手順

To a stirring suspension of 4-(4-pyridyl)benzoic acid (0.2 g, 1 mmol) in toluene (35 mL) was added thionyl chloride (0.55 mL, 7.5 mmol) and the mixture was heated to reflux. After 1 h the solution was cooled and added to a solution of 2-amino-N-(4-methoxyphenyl)benzamide (0.176 g, 0.73 mmol) in pyridine (2 mL) and toluene (5 mL). After stirring for 48 h, the solvent was removed in vacuo and the residue was partitioned between ethyl acetate and water. The organic phase was separated and washed with sat. NaHCO3, brine and dried (MgSO4), filtered and concentrated to give 103 mg of brown solid which was chromatographed by RPHPLC Method B. Upon standing, a sample of the title compound (14 mg, 4%) crystalized from one of the product containing fractions.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06605626B2
出典データセットuspto-grants-2003_08
ORD IDord-f64df43c3e664dbc9dab3e6aa122d8da
出典メモuspto-grants-2003_08