2,6-Lutidine → 2-Amino-4-ethynyl-thiophene-3-carboxylic acid ethyl ester
반응식
[CH2:1]([O:3][C:4]([C:6]1[C:10]([C:11]#[CH:12])=[CH:9][S:8][C:7]=1[NH:13]C(OC(C)(C)C)=O)=[O:5])[CH3:2].N1C(C)=CC=CC=1C.FC(F)(F)S(O[Si](C(C)(C)C)(C)C)(=O)=O.[NH4+].[Cl-].[F-].C([N+](CCCC)(CCCC)CCCC)CCC>C(Cl)Cl>[CH2:1]([O:3][C:4]([C:6]1[C:10]([C:11]#[CH:12])=[CH:9][S:8][C:7]=1[NH2:13])=[O:5])[CH3:2]참가 물질
반응물 5
생성물 1
시약·촉매·용매 1
실험 절차
2-t-Butoxycarbonylamino-4-ethynyl-thiophene-3-carboxylic acid ethyl ester (5.86 g, 19.85 mmol) was dissolved in anhydrous CH2Cl2 (125 mL). This was treated with 2,6-lutidine (4.62 mL, 39.70 mmol) followed by dropwise addition of t-butyldimethylsilyl trifluoromethanesulfonate (6.84 mL, 29.77 mmol). This was stirred at room temperature for 2 hr. Next it was poured into sat. NH4Cl (100 mL) and then extracted with EtOAc (3×100 mL). The combined extracts were washed with H2O (1×100 mL), and brine (1×100 mL). The organic layer was dried (Na2SO4), filtered and the solvent removed in vacuo. The residue was dissolved in anhydrous THF (85 mL) and treated with tetrabutylammonium fluoride (19.85 mL, 19.85 mmol, 1 M in THF). The reaction was then stirred at room temperature for 1 hr. The reaction was poured into sat. NH4Cl (100 mL) and then extracted with EtOAc (3×100 mL). The combined extracts were washed with H2O (1×100 mL), and brine (1×100 mL). The extracts were dried (Na2SO4), filtered and the solvent removed in vacuo. The crude product was purified by flash chromatography (SiO2, 1 EtOAc/9 hexanes) to afford the title compound (3.0 g, 77%). MS m/e (CI) 196.0 (M+H)+; 1H NMR (300 MHz, CDCl3): δ ppm 1.38 (t, 2H), 3.07 (s, 1H), 4.32 (q, 2H), 6.04 (s, 2H), 6.54 (s, 1H), 7.26 (s, 1H); MS m/e (CI) 196.0 (M+H)+.
후처리
- extractionextracted with EtOAc (3×100 mL)
- washThe combined extracts were washed with H2O (1×100 mL), and brine (1×100 mL)
- dry with materialThe organic layer was dried (Na2SO4)
- filtrationfiltered
- customthe solvent removed in vacuo
- dissolutionThe residue was dissolved in anhydrous THF (85 mL)
- stirringThe reaction was then stirred at room temperature for 1 hr
- extractionextracted with EtOAc (3×100 mL)
- washThe combined extracts were washed with H2O (1×100 mL), and brine (1×100 mL)
- dry with materialThe extracts were dried (Na2SO4)
- filtrationfiltered
- customthe solvent removed in vacuo
- customThe crude product was purified by flash chromatography (SiO2, 1 EtOAc/9 hexanes)
출처 및 근거
- ORD 기록
- ord-3454b7e8170642b889d08e7572d20473
- 출처 데이터셋
- uspto-grants-2006_10
- 특허 번호
- US07119205B2
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