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HRID 339522作成日:2026年10月26日

Thionyl Chloride → 2-Trifluoromethyl-n-[4-(6-methoxy-1,3-benzothiazol-2-yl)phenyl]-4-(methoxy)benzamide

https://huagongshe.com/reaction/339522

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4-(6-Methoxy-1,3-benzothiazol-2-yl)anilineHCID 391870—
反応物4-methoxy-2-(trifluoromethyl)benzoic AcidHCID 2775294—
反応物4-Methoxy-3-(trifluoromethyl)benzoyl chlorideHCID 2775298—
溶媒PyridineHCID 1049—
生成物2-Trifluoromethyl-n-[4-(6-methoxy-1,3-benzothiazol-2-yl)phenyl]-4-(methoxy)benzamideHCID 6724046046%

反応手順

A stirred mixture of 4-methoxy-2-trifluoromethylbenzoic acid (0.50 g, 2.27 mmol) and thionyl chloride (9 ml) was heated under reflux for 4 h. After cooling to room temperature, the excess reagent was removed under reduced pressure to give crude acid chloride. The amide was prepared as described in the Amide Coupling section using the crude 4-methoxy-5-trifluoromethylbenzoyl chloride and 2-(4-aminophenyl)-6-methoxybenzo thiazole (0.58 g, 2.27 mmol) in dry pyridine (15 ml) to give the title compound (0.478 g, 46%) as pale yellow needles after work-up and recrystallisation from acetic acid.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08895313B2
出典データセットuspto-grants-2014_11
ORD IDord-d3daccfe68cc4410bdbac4b9d5eab2e2
出典メモuspto-grants-2014_11