Methyl iodide → N-Methyl-5-(trifluoromethyl)thiophen-2-amine

HRID 588068노트

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HRID 588068 반응식
[F:1][C:2]([F:17])([F:16])[C:3]1[S:7][C:6]([NH:8][C:9](=O)OC(C)(C)C)=[CH:5][CH:4]=1.[H-].[Na+].CI.FC(F)(F)C(O)=O>CN(C=O)C.C(Cl)Cl>[CH3:9][NH:8][C:6]1[S:7][C:3]([C:2]([F:17])([F:1])[F:16])=[CH:4][CH:5]=1

참가 물질

7

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온도
0 °C

실험 절차

To tert-butyl 5-(trifluoromethyl)thiophen-2-ylcarbamate (0.40 g, 1.5 mmol) in DMF (9 mL) at 0° C. was added NaH (72 mg, 1.8 mmol, 60% dispersion in mineral oil) in one portion. After 40 minutes MeI (0.20 mL, 1.8 mmol) was added via syringe. After stirring for 30 minutes at 0° C., TLC of a quenched aliquot showed the reaction was complete. The reaction was quenched by pouring into a biphasic mixture of 1N HCl and EtOAc. The layers were separated, and the organic layer was washed 3× with H2O, 1× with brine, dried over MgSO4, filtered, and concentrated under reduced pressure to afford a yellow oil. The crude oil was added to CH2Cl2 (2 mL) and trifluoroacetic acid (2 mL). After this mixture had been stirred at ambient temperature for 80 minutes, TLC showed the reaction was complete. The solvents were removed under reduced pressure and the residue was taken up in CH2Cl2 and was washed with NaHCO3 aq sat. This aqueous wash was back extracted 1× with CH2Cl2, then the combined organic layers were dried over MgSO4, filtered, and concentrated under reduced pressure. N-Methyl-5-(trifluoromethyl)thiophen-2-amine was used directly in the next step.

후처리

  1. customThe reaction was quenched
  2. additionby pouring into a biphasic mixture of 1N HCl and EtOAc
  3. customThe layers were separated
  4. washthe organic layer was washed 3× with H2O, 1× with brine
  5. dry with materialdried over MgSO4
  6. filtrationfiltered
  7. concentrationconcentrated under reduced pressure
  8. customto afford a yellow oil
  9. stirringAfter this mixture had been stirred at ambient temperature for 80 minutes
  10. customThe solvents were removed under reduced pressure
  11. washwas washed with NaHCO3 aq sat.
  12. washThis aqueous wash
  13. extractionwas back extracted 1× with CH2Cl2
  14. dry with materialthe combined organic layers were dried over MgSO4
  15. filtrationfiltered
  16. concentrationconcentrated under reduced pressure

출처 및 근거

ORD 기록
ord-ea16d65a7c9b4a0fa6c7121826202783
출처 데이터셋
uspto-grants-2016_01
특허 번호
US09227957B2

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