関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Sodium Carbonate | HCID 10340 | — |
| 反応物 | Toluene ethanol | HCID 21863594 | — |
| 反応物 | tert-Butyl (5-methyl-2-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)carbamate | HCID 46737997 | — |
| 反応物 | Ethyl 5-chloro-6-cyanonicotinate | HCID 66875248 | — |
| 溶媒 | Methanol | HCID 887 | — |
| 生成物 | Ethyl 5-amino-8-methylbenzo[f][1,7]naphthyridine-2-carboxylate | HCID 58213495 | — |
反応手順
A solution of tert-butyl 5-methyl-2-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenylcarbamate (from Example 5/step 2) (1.0 eq.) and ethyl 5-chloro-6-cyanonicotinate (from the previous step) (1.0 eq.), tetrakis(triphenyl-phosphine)palladium (5 mol %), and 2N aqueous sodium carbonate solution (2.0 eq.) in toluene/ethanol (2:1, 0.03 M) was stiffed at 100° C. overnight. After cooling to ambient temperature, the reaction content was diluted with methanol. The insoluble solids were filtered off, and the filtrate was concentrated en vacuo to obtain a crude residue. The crude material was purified by flash chromatography on a COMBIFLASH® system (ISCO) using 0-80% ethyl acetate in hexane to give ethyl 5-amino-8-methylbenzo[f][1,7]naphthyridine-2-carboxylate.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US08895577B2 |
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| 出典データセット | uspto-grants-2014_11 |
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| ORD ID | ord-0a2ce5a7b8994d76afc20305b6ccc0b3 |
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| 出典メモ | uspto-grants-2014_11 |
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