関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Cyclopropylboronic acid | HCID 2760897 | — |
| 反応物 | 6-Bromo-3,4-dihydro-2H-isoquinolin-1-one | HCID 21865450 | — |
| 触媒 | Tricyclohexylphosphine | HCID 75806 | — |
| 触媒 | palladium(II) acetate | HCID 167845 | — |
| 溶媒 | Water | HCID 962 | — |
| 溶媒 | Toluene | HCID 1140 | — |
| 生成物 | 6-cyclopropyl-3,4-dihydro-2H-isoquinolin-1-one | HCID 57424117 | 97.2% |
反応手順
To a round bottomed flask charged with 6-Bromo-3,4-dihydro-2H-isoquinolin-1-one (16.9 g, 74.7 mmol), cyclopropylboronic acid (9.45 g, 1.5 equiv), tricyclohexylphosphine (1.04 mg, 0.025 equiv), and K3PO4 hexahydrate (50 g, 2 equiv) in toluene (210 mL) and H2O (15 mL) was added Pd(OAc)2 (100 mg, 0.05 equiv). The combined mixture was heated for 4 h at 100° C. The reaction mixture was cooled, filtered and washed with toluene. The organic phase was partitioned and washed with water and brine, dried over Na2SO4, filtered and concentrated to an oil. Addition of hexanes produced 6-Cyclopropyl-3,4-dihydro-2H-isoquinolin-1-one as a tan solid (13.6 g). MS (ESI) 187.1 (M+H)+.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US07683064B2 |
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| 出典データセット | uspto-grants-2010_03 |
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| ORD ID | ord-0a49f5aba82e44988653de65197e32d8 |
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| 出典メモ | uspto-grants-2010_03 |
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