Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
Iodine → (Rac)-6-chloro-3-[1-(3-methyl-3h-benzoimidazol-5-yl)-ethyl]-imidazo[1,2-b]pyridazine
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | Iodine | HCID 807 | — |
| 반응물 | Sodium Hydroxide | HCID 14798 | — |
| 반응물 | Sodium Bicarbonate | HCID 516892 | — |
| 반응물 | Phosphinic Acid | HCID 4124402 | — |
| 반응물 | (Rac)-1-(6-chloro-imidazo[1,2-b]pyridazin-3-yl)-1-(3-methyl-3h-benzoimidazol-5-yl)-ethanol | HCID 87523187 | — |
| 용매 | Acetic Acid | HCID 176 | — |
| 용매 | Water | HCID 962 | — |
| 생성물 | (Rac)-6-chloro-3-[1-(3-methyl-3h-benzoimidazol-5-yl)-ethyl]-imidazo[1,2-b]pyridazine | HCID 87524205 | — |
반응 단계
In a microwave vial, (rac)-1-(6-chloro-imidazo[1,2-b]pyridazin-3-yl)-1-(3-methyl-3H-benzoimidazol-5-yl)-ethanol (Stage 185.3, 650 mg, 1.507 mmol) was dissolved in AcOH (15 mL) under Argon. Iodine (1.148 g, 4.52 mmol) and H3PO2 (1.233 mL of a 50% aqueous solution, 11.3 mmol) were added and the mixture was submitted to MW-irradiation at 150° C. for 10 min. The mixture was diluted with water. It was basified until pH 5 with NaOH 10 M and then saturated NaHCO3 sol. until pH 7-8. It was then extracted with EtOAc one time. The organic phase was washed with brine, dried over Na2SO4, filtered and evaporated. It was then dried under vacuum overnight to afford the title compound as a foam (tR 2.12 min (conditions 8), MH+=312).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US08822468B2 |
| 출처 데이터셋 | uspto-grants-2014_09 |
| ORD ID | ord-07e1d19cae974f2cbf4f07c9c5193403 |
| 출처 메모 | uspto-grants-2014_09 |