참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | 1,1'-Thiocarbonyldi-2(1H)-pyridone | HCID 853162 | — |
| 반응물 | 6-fluoro-1H-indazol-3-amine | HCID 21939267 | — |
| 용매 | Dichloromethane | HCID 6344 | — |
| 생성물 | HCID 178505448 | HCID 178505448 | 73% |
반응 단계
To 6-fluoro-1H-indazol-3-amine (0.32 g, 2.1 mmol) in dichloromethane (15 mL) was added 1,1′-thiocarbonyldipyridin-2(1H)-one (0.53 g, 2.30 mmol). The reaction was stirred at 50° C. for 3 hours. The reaction was cooled to room temperature and the crude product was purified by column chromatography (25% ethyl acetate/hexanes) to afford 6-fluoro-3-isothiocyanato-1H-indazole (0.30 g, 1.53 mmol, 73.0% yield) as a light yellow powder. 1H NMR (500 MHz, DMSO-D6) δ ppm 13.39 (s, 1 H), 7.78 (dd, J=8.85, 4.88 Hz, 1 H), 7.41 (dd, J=9.31, 1.68 Hz, 1 H), 7.14 (td, J=9.16, 1.83 Hz, 1 H). MS (LC/MS) R.T.=3.69; [M+H]+=194.07.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US07863291B2 |
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| 출처 데이터셋 | uspto-grants-2011_01 |
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| ORD ID | ord-e0ee9f76af004c94842fb35a16627a91 |
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| 출처 메모 | uspto-grants-2011_01 |
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