참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Trichloroacetonitrile | HCID 11011 | — |
| 반응물 | 4-(Dimethylamino)benzoic acid | HCID 12092 | — |
| 반응물 | HCID 178418824 | HCID 178418824 | — |
| 용매 | Acetonitrile | HCID 6342 | — |
| 생성물 | Dimethyl-(4-oxazolo[5,4-b]pyridin-2-yl-phenyl)-amine | HCID 22754785 | 6.7% |
반응 단계
3-Amino-pyridin-2-ol (50 mg, 0.45 mmol), 4-dimethylamino-benzoic acid (74 mg, 0.45 mmol), trichloroacetonitrile (91 μL, 0.91 mmol), and polystyrene triphenylphosphine (425 mg, 1.362 mmol) were suspended in acetonitrile (4.5 mL) and heated by microwave to 150° C. for 15 min. The crude reaction mixture was filtered and concentrated affording a residue which was purified by reverse phase chromatography affording dimethyl-(4-oxazolo[5,4-b]pyridin-2-yl-phenyl)-amine (7.1 mg, 0.030 mmol, 6.6% yield). ES MS (M+H+)=240; 1H NMR (300 MHz, CDCl3): δ 8.24 (d, J=5.1 Hz, 1H); 8.14 (d, J=8.6 Hz, 2H); 7.95 (d, J=7.8 Hz, 1H); 7.28 (dd, J=7.7, 4.9 Hz, 2H); 6.78 (d, J=8.6 Hz, 1H); 3.09 (s, 6H); HRMS m/z 240.1122 (C14H13N3O1+H+ requires 240.1132).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US08530483B2 |
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| 출처 데이터셋 | uspto-grants-2013_09 |
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| ORD ID | ord-3daf2858d8c249759d5a0b398ac9e5f0 |
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| 출처 메모 | uspto-grants-2013_09 |
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