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HRID 561979作成日:2026年10月25日
Potassium Carbonate → {(1S,2S)-1-[5-(2-fluoro-phenyl)-1H-imidazol-2-yl]-2-phenyl-propyl}-carbamic acid tert-butyl ester
https://huagongshe.com/reaction/561979
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Potassium Carbonate | HCID 11430 | — |
| 反応物 | Cyclopropylboronic acid | HCID 2760897 | — |
| 反応物 | Water ethanol | HCID 19096565 | — |
| 反応物 | {(1S,2S)-1-[5-(2-fluoro-4-iodo-phenyl)-1H-imidazol-2-yl]-2-phenyl-propyl}-carbamic acid tert-butyl ester | HCID 67001487 | — |
| 触媒 | Dichlorobis(tricyclohexylphosphine)pallium (II) | HCID 11050900 | — |
| 溶媒 | Toluene | HCID 1140 | — |
| 溶媒 | Ethyl Acetate | HCID 8857 | — |
| 生成物 | {(1S,2S)-1-[5-(2-fluoro-phenyl)-1H-imidazol-2-yl]-2-phenyl-propyl}-carbamic acid tert-butyl ester | HCID 67001749 | 107.1% |
反応手順
To a degassed mixture of {(1S,2S)-1-[5-(2-fluoro-4-iodo-phenyl)-1H-imidazol-2-yl]-2-phenyl-propyl}-carbamic acid tert-butyl ester (150 mg, 0.288 mmol) in toluene (5 mL) and 1:1 v/v deionized water/ethanol (2 mL) were added dichlorobis(tricyclohexylphosphine)palladium(II) (6.4 mg, 0.009 mmol), cyclopropylboronic acid (27 mg, 0.314 mmol), potassium carbonate (159 mg, 1.15 mmol) and the mixture refluxed for 3 hours under an atmosphere of nitrogen. The mixture was diluted with ethyl acetate (50 mL) and washed with water (50 mL). The aqueous layer was washed with ethyl acetate (50 mL) and the combined organic extracts were washed with brine, dried over sodium sulfate, filtered and concentrated in vacuo. The crude product was purified by chromatography over silica gel gradient eluted between 0 and 40% v/v ethyl acetate in hexanes to give {(1S,2S)-1-[5-(2-fluoro-phenyl)-1H-imidazol-2-yl]-2-phenyl-propyl}-carbamic acid tert-butyl ester (122 mg, 107%) which was then used in step 17-G. HR-MS: calcd for C29H27FN4O4 [M+H+] 515.2089. Found 515.2089.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US08063085B2 |
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| 出典データセット | uspto-grants-2011_11 |
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| ORD ID | ord-638386412380420698f1d02379bb4263 |
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| 出典メモ | uspto-grants-2011_11 |
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