関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Methyl chloroformate | HCID 6586 | — |
| 反応物 | Lithium diisopropylamide | HCID 2724682 | — |
| 反応物 | 7-bromo-2-methyl-2H-indazole | HCID 21094580 | — |
| 反応物 | Tetrahydrofuran heptane ethylbenzol | HCID 22742125 | — |
| 生成物 | Methyl 7-bromo-2-methyl-2H-indazole-3-carboxylate | HCID 58861011 | 79.3% |
反応手順
To a solution of 7-bromo-2-methyl-2H-indazole (6: R=Me, 1.50 g, 7.12 mmol) in 50 mL of THE at −78° C. was added a 2 M solution of lithium diisopropylamide in THF/heptane/ethylbenzene (4.3 mL, 8.6 mmol). The solution was stirred at 0-5° C. for 15 m, then rechilled to −78° C. To the solution was added methyl chloroformate (0.66 mL, 8.5 mmol) all at once, and the mixture was stirred while slowly warmed to room temperature over 19 h. The reaction was quenched with silica gel and concentrated. Column chromatography (0→20% EtOAc/hexanes) afforded of 7-bromo-2-methyl-2H-indazole-3-carboxylic acid methyl ester (35a: 1.52 g; 79%; m.p. 131-132) as a pale yellow solid.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US07365211B2 |
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| 出典データセット | uspto-grants-2008_04 |
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| ORD ID | ord-3c162ef834344c9ab173b70193a78db0 |
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| 出典メモ | uspto-grants-2008_04 |
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