関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Sodium Carbonate | HCID 10340 | — |
| 反応物 | 5'-Bromospiro[1,3-dioxolane-2,3'-[3H]indol]-2'(1'H)-one | HCID 2732922 | — |
| 反応物 | 3,5-Dimethylisoxazole-4-boronic acid | HCID 2734346 | — |
| 触媒 | Dichloro[1,1'-bis(di-tert-butylphosphino)ferrocene]palladium(II) | HCID 53384307 | — |
| 溶媒 | 1,4-Dioxane--water (1/1) | HCID 21886435 | — |
| 生成物 | 5'-(3,5-Dimethylisoxazol-4-yl)spiro[[1,3]dioxolane-2,3'-indolin]-2'-one | HCID 117668384 | 60.2% |
反応手順
A mixture of 3,5-dimethylisoxazol-4-ylboronic acid (159 g, 1.13 mol), dichloro[1,1′-bis(di-tert-butylphosphino)ferrocene]palladium(II) (23.6 g, 29 mmol), 5′-bromospiro[[1,3]dioxolane-2,3′-indolin]-2′-one (236 g, 0.87 mol) and Na2CO3 (184 g, 1.7 mol) in dioxane/H2O (1200 mL/300 mL) was heated to 110° C. for 12 h. The mixture was filtered through a pad of celite and concentrated in vacuo. The crude product was dissolved in CH2Cl2 (2 L), then hexane 2 L was added and the mixture was filtered again, the organic phase was concentrated in vacuo to give target product (150 g, 60%). 1H NMR (400 MHz, DMSO-d6): δH 10.56 (s, 1H), 7.31-7.33 (m, 2H), 6.93 (d, J=8.0 Hz, 1H), 4.27-4.35 (m, 4H), 2.35 (s, 3H), 2.18 (s, 3H). MS (ESI) m/e [M+1]+ 287.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US09393232B2 |
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| 出典データセット | uspto-grants-2016_07 |
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| ORD ID | ord-72e7937554db43e59b6e0687f4539861 |
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| 出典メモ | uspto-grants-2016_07 |
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