1-Fluoro-4-(methylsulphonyl)benzene → [1,2,4]Triazolo[1,5-a]pyridin-2-amine
반응식
[NH2:1][C:2]1[N:11]=[C:5]2[C:6](O)=[CH:7][CH:8]=[CH:9][N:4]2[N:3]=1.FC1C=CC(S(C)(=O)=O)=CC=1.CC(C)([O-])C.[K+]>CN(C)C(=O)C>[N:11]1[C:2]([NH2:1])=[N:3][N:4]2[CH:9]=[CH:8][CH:7]=[CH:6][C:5]=12참가 물질
반응 조건
- 온도
- 130 °C
실험 절차
A well stirred mixture of 2-amino-[1,2,4]triazolo[1,5-a]pyridine-8-ol (0.300 g, 2.00 mmol), 1-fluoro-4-methanesulfonyl-benzene (0.418 g, 2.40 mmol), N,N-dimethylacetamide (2 mL) and potassium tert-butoxide (0.448 g, 4.00 mmol) was heated at 130° C. for 18 h under an argon atmosphere. The reaction mixture was evaporated in vacuo and partitioned between dichloromethane and saturated aqueous sodium bicarbonate solution. The aqueous phase was extracted twice with dichloromethane and the combined organic layers were washed with brine, dried over sodium sulfate, filtered, and evaporated in vacuo to furnish a crude product. The crude product was purified by preparative Gilson HPLC method to yield a pure product, which was triturated from a mixture of dichloromethane, methanol, ether and hexane. 8-(4-Methanesulfonyl-phenoxy)-[1,2,4-triazolo[1,5-a]pyridin-2-ylamine was isolated as a white solid (125 mg, 20%). MP=245-247° C. 1H NMR (400 MHz, (D3C)2SO, δ, ppm): 8.53 (d, J=6.56 Hz, 1H), 7.87 (d, J=8.77 Hz, 2H), 7.36 (d, J=7.73 Hz, 1H), 7.15 (d, J=8.76 Hz, 2H), 6.92 (t, J=7.28 Hz, 1H), 6.13 (s, 1H), 3.19 (s, 3H). MS=305 (MH)+.
후처리
- customThe reaction mixture was evaporated in vacuo
- custompartitioned between dichloromethane and saturated aqueous sodium bicarbonate solution
- extractionThe aqueous phase was extracted twice with dichloromethane
- washthe combined organic layers were washed with brine
- dry with materialdried over sodium sulfate
- filtrationfiltered
- customevaporated in vacuo
- customto furnish a crude product
- customThe crude product was purified by preparative Gilson HPLC method
- customto yield a pure product, which
- customwas triturated from a mixture of dichloromethane, methanol, ether and hexane
출처 및 근거
- ORD 기록
- ord-71c331633c1648f7bf48034a61817c22
- 출처 데이터셋
- uspto-grants-2014_01
- 특허 번호
- US08633173B2
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