Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
4-Iodo-1-tritylimidazole → 1-isoquinolin-1-yl-1-(1-trityl-1H-imidazol-4-yl)-ethanol
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | 4-Iodo-1-tritylimidazole | HCID 618252 | — |
| 반응물 | 1-(Isoquinolin-1-yl)ethan-1-one | HCID 13157214 | — |
| 반응물 | HCID 178418443 | HCID 178418443 | — |
| 용매 | Dichloromethane | HCID 6344 | — |
| 생성물 | 1-isoquinolin-1-yl-1-(1-trityl-1H-imidazol-4-yl)-ethanol | HCID 59751483 | — |
반응 단계
A mixture of 4-iodo-1-tritylimidazole (commercially available) (15.5 g, 35.4 mmol) in dichloromethane (80 mL) at 20° C. was treated with ethyl magnesium bromide (12.0 mL, 36 mmol, 3M in ether) and allowed to react for 1 h. A solution of 1-isoquinolin-1-yl-ethanone (Intermediate H2) (3.65 g, 21.3 mmol) in dichloromethane (20 mL) was added via addition funnel at 20° C. and stirred for 16 h. The mixture was quenched with sat. ammonium chloride (100 mL) and diluted with dichloromethane. The residue was isolated in an aqueous workup. The product was extracted with CH2Cl2 and purified by chromatography on silica gel with 5% NH3-MeOH: CH2Cl2 to give 1-isoquinolin-1-yl-1-(1-trityl-1H-imidazol-4-yl)-ethanol (Intermediate H3) as a solid.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US07399868B2 |
| 출처 데이터셋 | uspto-grants-2008_07 |
| ORD ID | ord-233ecd94c5474dd7a7ef2c8171474ec3 |
| 출처 메모 | uspto-grants-2008_07 |