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HRID 2421246作成日:2026年10月25日
Potassium Phosphate, Tribasic → 1-{3,5-difluoro-4-[(phenylmethyl)oxy]phenyl}-4-[(phenylmethyl)oxy]-1H-indole
https://huagongshe.com/reaction/2421246
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Potassium Phosphate, Tribasic | HCID 62657 | — |
| 反応物 | 4-(phenylmethoxy)-1H-indole | HCID 88465 | — |
| 反応物 | L-Proline | HCID 145742 | — |
| 反応物 | 4-Bromo-2,6-difluoro-1-(benzyloxy)benzene | HCID 14207641 | — |
| 溶媒 | Dimethylformamide | HCID 6228 | — |
| 生成物 | 1-{3,5-difluoro-4-[(phenylmethyl)oxy]phenyl}-4-[(phenylmethyl)oxy]-1H-indole | HCID 59627928 | — |
反応手順
4-[(phenylmethyl)oxy]-1H-indole (500 mg, 2.24 mmoL), 4-bromo-2,6-difluorophenyl phenylmethyl ether (prepared as described in part a), 559 mg, 1.87 mmoL), K3PO4 (990 mg, 4.67 mmoL) and L-Proline (43 mg, 0.373 mmoL) were dissolved in DMF (5 mL) in a microwave vial and degassed by sonication under a flow of argon. To this was added CuI (71 mg, 0.373 mmoL) and the solution was heated to 140° C. in the microwave reactor. After 3 hours the mixture was partitioned between ethyl acetate (100 mL)/water (100 mL), the phases were separated and the aqueous phase re-extracted with ethyl acetate (100 mL). The combined organic phases were washed with sat. NH4Cl (2×100 mL), water (100 mL) and brine (2×100 mL) and finally dried over MgSO4. The crude product was purified by flash chromatography (Biotage SP4, 40+S Cartridge) eluting with a gradient of 0 to 20% Et2O in hexane to give the title compound (D21), (299 mg).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US07956083B2 |
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| 出典データセット | uspto-grants-2011_06 |
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| ORD ID | ord-21b4da8f52ec452fbd78b8ee88eef7e4 |
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| 出典メモ | uspto-grants-2011_06 |
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