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6-Amino-3-oxo-2,3-dihydro-indazole-1-carboxylic acid tert-butyl ester → HCID 178518844、化合物
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | 6-Amino-3-oxo-2,3-dihydro-indazole-1-carboxylic acid tert-butyl ester | HCID 57498019 | — |
| 反応物 | HCID 178526632 | HCID 178526632 | — |
| 生成物 | HCID 178518844 | HCID 178518844 | 16.2% |
反応手順
6-[6-(5-Cyclopropyl-2H-pyrazol-3-ylamino)-5-nitro-pyridin-2-ylamino]-1,2-dihydro-indazol-3-one was prepared by the reaction of (6-Chloro-3-nitro-pyridin-2-yl)-(5-cyclopropyl-2H-pyrazol-3-yl)-amine and 6-Amino-3-oxo-2,3-dihydro-indazole-1-carboxylic acid tert-butyl ester in a similar manner as described above to afford 17 mg of the desired product as a bright yellow solid (16.2% yield). H-NMR (CD3OD) δ 8.32(d, 1H), 7.68(d, 1H), 7.65(s, 1H), 7.17(d, 1H), 6.38(d, 1H), 6.24(s, 1H), 1.79(m, 1H), 0.84(m, 2H), 0.48(m, 2H). MS (ES+): m/e=393.2 (M+H), 391.2 (M−H); LC/Method A/4.149 min, 100% purity by area %.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US07262200B2 |
| 出典データセット | uspto-grants-2007_08 |
| ORD ID | ord-807cfa47c6224515ae0afbdfeb6414c1 |
| 出典メモ | uspto-grants-2007_08 |