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HRID 42306作成日:2026年10月25日

Thiobenzamide → 2-Phenyl-4-(2-phenylpyrimidin-5-yl)thiazole

https://huagongshe.com/reaction/42306

反応式

関与物質

役割名称HCID仕込み量
反応物ThiobenzamideHCID 683563—
反応物2-Bromo-1-(2-phenylpyrimidin-5-yl)ethanoneHCID 59252454—
溶媒EthanolHCID 702—
生成物2-Phenyl-4-(2-phenylpyrimidin-5-yl)thiazoleHCID 5925244746%

反応手順

A mixture consisting of 2-bromo-1-(2-phenylpyrimidin-5-yl)ethanone (Example 14, Step B, 50 mg, 0.18 mmol), thiobenzamide (TCl America, 25 mg, 0.18 mmol) and absolute ethanol (4 mL) in a capped scintillation vial was heated to near boiling for several minutes and was subsequently allowed to cool to room temperature. A white solid precipitated within minutes. The precipitate was collected by vacuum filtration. Light ethanol rinse, suction, and drying under high vacuum at room temperature afforded the title compound (26 mg, 46% yield) as an off-white solid; melting point 214.4-216.1° C.; 1H-NMR (400 MHz; DMSO-d6) δ 9.54 (s, 2H), 8.54 (s, 1H), 8.47 (m, 2H), 8.08 (m, 2H), 7.62-7.54 (m, 6H); LC/MS (ESI+) m/z 316.1, (ESI−) m/z 337.2 (M−1+Na+); H-PGDS FPBA IC50: >20 μM.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08536185B2
出典データセットuspto-grants-2013_09
ORD IDord-59b63460ac33409aa614d4fadb29ae68
出典メモuspto-grants-2013_09