참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Acefylline | HCID 69550 | — |
| 반응물 | 2-(4-Aminophenyl)propan-2-ol | HCID 9543261 | — |
| 반응물 | Methanaminium, N-((dimethylamino)(3H-1,2,3-triazolo(4,5-b)pyridin-3-yloxy)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1) | HCID 9886157 | — |
| 용매 | N,N-dimethylformamide; methylsulfinylmethane | HCID 3013483 | — |
| 생성물 | HCID 45254481 | HCID 45254481 | — |
반응 단계
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.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US08541423B2 |
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| 출처 데이터셋 | uspto-grants-2013_09 |
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| ORD ID | ord-baba062cb47f4c34aaf02c30011c1cd1 |
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| 출처 메모 | uspto-grants-2013_09 |
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