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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 42306생성일: 2026년 10월 24일

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

https://huagongshe.com/ko/reaction/42306

반응식

참여 물질

역할이름HCID투입량
반응물ThiobenzamideHCID 683563—
반응물2-Bromo-1-(2-phenylpyrimidin-5-yl)ethanoneHCID 59252454—
용매EthanolHCID 702—
생성물2-Phenyl-4-(2-phenylpyrimidin-5-yl)thiazoleHCID 5925244746%

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08536185B2
출처 데이터셋uspto-grants-2013_09
ORD IDord-59b63460ac33409aa614d4fadb29ae68
출처 메모uspto-grants-2013_09