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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 900982생성일: 2026년 10월 24일

3,4-Thiophenediacetonitrile, 2,5-dimethyl- → [2,5-Dimethyl-4-(4,5,7-trifluoro-benzothiazol-2-ylmethyl)-thiophen-3-yl]-acetonitrile

https://huagongshe.com/ko/reaction/900982

반응식

참여 물질

역할이름HCID투입량
반응물3,4-Thiophenediacetonitrile, 2,5-dimethyl-HCID 819018—
반응물Benzenethiol, 2-amino-3,4,6-trifluoro-, hydrochlorideHCID 11390282—
용매EthanolHCID 702—
생성물[2,5-Dimethyl-4-(4,5,7-trifluoro-benzothiazol-2-ylmethyl)-thiophen-3-yl]-acetonitrileHCID 5969881331.2%

반응 단계

A solution of (4-cyanomethyl-2,5-dimethyl-thiophen-3-yl)-acetonitrile (1.90 g, 10.0 mmol) and 2-amino-3,4,6-trifluoro-benzenethiol hydrochloride (2.16 g, 10.0 mmol) in EtOH (22 mL) is heated to reflux for 44 h. After cooling to room temperature, the mixture is concentrated in vacuo and purified by flash chromatography (silica gel, 10-30% ethyl acetate in heptane). Further purification by recrystallization with ethyl acetate and heptane gave [2,5-dimethyl-4-(4,5,7-trifluoro-benzothiazol-2-ylmethyl)-thiophen-3-yl]-acetonitrile (1.1 g, 31.2%) as a white powder: mp 145-146° C.; Rf 0.54 (30% ethyl acetate in heptane); 1H NMR (CDCl3, 300 MHz) δ 6.95-7.08 (m, 1 H), 4.36 (s, 2 H), 3.59 (s, 2 H), 2.43 (s, 3 H), 2.41 (s, 3 H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07361671B2
출처 데이터셋uspto-grants-2008_04
ORD IDord-c767adab3d1a47d98d79fc17ebadb3bd
출처 메모uspto-grants-2008_04