関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Diisopropylethylamine | HCID 81531 | — |
| 反応物 | 3-Methylpicolinic acid | HCID 268757 | — |
| 反応物 | Methanaminium, N-((dimethylamino)(3H-1,2,3-triazolo(4,5-b)pyridin-3-yloxy)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1) | HCID 9886157 | — |
| 反応物 | HCID 178507273 | HCID 178507273 | — |
| 溶媒 | Dimethylformamide | HCID 6228 | — |
| 生成物 | Ammonia methanol | HCID 21705897 | — |
| 生成物 | HCID 178426298 | HCID 178426298 | 13.3% |
反応手順
To 3-Methyl-2-pyridinecarboxylic acid (0.032 g, 0.234 mmol) in DMF (0.5 ml) was added HATU (0.089 g, 0.234 mmol) and the solution stirred for 10 min at 20° C. To this was then added a solution of 3-fluoro-6-(1H-indol-4-yl)-1H-indazol-4-amine (0.052 g, 0.195 mmol) in DMF (0.5 ml), followed by DIPEA (0.068 ml, 0.391 mmol) and the top was placed on the vial which had been pierced with a needle. The mixture was stirred at 20° C. for 66 hours then loaded directly onto a dry 1 g NH2 cartridge, left for 2 hours then eluted with methanol (2.5 column vols). Upon standing for 20 hours at 20° C., a solid precipitated from the orange solution which was filtered off and dried. The solid was triturated with methanol (2×2 ml) then blown to dryness and loaded onto a 500 mg SCX pre-rinsed with methanol. Elution with methanol (3 column vols) then 2M NH3/MeOH (3 column vols) and concentration of the basic fractions by blow down afforded the title compound (6 mg).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US08765743B2 |
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| 出典データセット | uspto-grants-2014_07 |
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| ORD ID | ord-fffd4132a77f4dc98301d614649637f9 |
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| 出典メモ | uspto-grants-2014_07 |
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