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4-Iodo-1-tritylimidazole → 1-isoquinolin-1-yl-1-(1-trityl-1H-imidazol-4-yl)-ethanol
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | 4-Iodo-1-tritylimidazole | HCID 618252 | — |
| 反応物 | 1-(Isoquinolin-1-yl)ethan-1-one | HCID 13157214 | — |
| 反応物 | HCID 178418443 | HCID 178418443 | — |
| 溶媒 | Dichloromethane | HCID 6344 | — |
| 生成物 | 1-isoquinolin-1-yl-1-(1-trityl-1H-imidazol-4-yl)-ethanol | HCID 59751483 | — |
反応手順
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.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US07399868B2 |
| 出典データセット | uspto-grants-2008_07 |
| ORD ID | ord-233ecd94c5474dd7a7ef2c8171474ec3 |
| 出典メモ | uspto-grants-2008_07 |