Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
Diisopropylamine → S-1-(4-Fluorophenyl)-1H-indazol-5-yl benzothioate
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | Diisopropylamine | HCID 7912 | — |
| 반응물 | 3,4,7,8-Tetramethyl-1,10-phenanthroline | HCID 74265 | — |
| 반응물 | 1-(4-fluorophenyl)-5-iodo-1H-indazole | HCID 59251128 | — |
| 반응물 | HCID 178526132 | HCID 178526132 | — |
| 촉매 | HCID 178505377 | HCID 178505377 | — |
| 용매 | Toluene | HCID 1140 | — |
| 용매 | Ethyl Acetate | HCID 8857 | — |
| 생성물 | S-1-(4-Fluorophenyl)-1H-indazol-5-yl benzothioate | HCID 59339848 | 20% |
반응 단계
To a solution of 1-(4-fluorophenyl)-5-iodo-1H-indazole (103e, 0.224 g, 0.66 mmol), thiobenzoic acid (0.093 ml, 0.79 mmol), 3,4,7,8-tetramethyl-1,10-phenantroline (0.031 g, 0.13 mmol) and N,N-diisopropylamine (0.220 ml, 1.32 mmol) in toluene (2.5 ml) was added copper(I) iodine (2.245 μl, 0.07 mmol). The resulting mixture was stirred at 110 C O/N. The reaction mixture was cooled to r.t. diluted with EtOAc and washed with water. The organic phase was the dried the solvent evaporated and then purified on HPLC. The relevant fractions were collected freezdried to give 45 mg of product (20% yield) which was analysed by LC/MS.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US07728030B2 |
| 출처 데이터셋 | uspto-grants-2010_06 |
| ORD ID | ord-5b1dc549e4134f18b2f42ea77cf3f868 |
| 출처 메모 | uspto-grants-2010_06 |