Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
3,4-Thiophenediacetonitrile, 2,5-dimethyl- → [2,5-Dimethyl-4-(4,5,7-trifluoro-benzothiazol-2-ylmethyl)-thiophen-3-yl]-acetonitrile
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | 3,4-Thiophenediacetonitrile, 2,5-dimethyl- | HCID 819018 | — |
| 반응물 | Benzenethiol, 2-amino-3,4,6-trifluoro-, hydrochloride | HCID 11390282 | — |
| 용매 | Ethanol | HCID 702 | — |
| 생성물 | [2,5-Dimethyl-4-(4,5,7-trifluoro-benzothiazol-2-ylmethyl)-thiophen-3-yl]-acetonitrile | HCID 59698813 | 31.2% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US07361671B2 |
| 출처 데이터셋 | uspto-grants-2008_04 |
| ORD ID | ord-c767adab3d1a47d98d79fc17ebadb3bd |
| 출처 메모 | uspto-grants-2008_04 |