関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Acefylline | HCID 69550 | — |
| 反応物 | 2-(4-Aminophenyl)propan-2-ol | HCID 9543261 | — |
| 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 | — |
| 溶媒 | N,N-dimethylformamide; methylsulfinylmethane | HCID 3013483 | — |
| 生成物 | HCID 45254481 | HCID 45254481 | — |
反応手順
To a 0° C. solution of acid 101 (0.32 g, 1.34 mmol) in DMF/DMSO (1:1, 20 mL) was added HATU (0.0.76 g, 2.01 mmol). The reaction was then stirred an additional 15 min at room temperature. The solution was cooled to 0° C. and amine 135 (0.30 g, 2.01 mmol) was added. The reaction was then stirred at rt overnight. The DMF was concentrated in vacuo and water was added to the reaction. The aqueous layer was extracted with EtOAc The ethyl acetate layer was then washed again with water and the organic layer was concentrated in vacuo. The product was purified by flash chromatography on silica gel eluting with EtOAc/hexanes and EtOAc/MeOH to yield 402 as a pure light brown semi solid (0.086 g, 17.5%). MS (APCI): m/z 372.2 [M−H]+ Anal. Calcd. For C18H21N5O4. 0.35 EtOAc: C, 57.93; H, 5.96; N, 17.41. Found C, 58.36; H, 6.14; N, 16.96.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US08541423B2 |
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| 出典データセット | uspto-grants-2013_09 |
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| ORD ID | ord-baba062cb47f4c34aaf02c30011c1cd1 |
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| 出典メモ | uspto-grants-2013_09 |
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