Potassium Iodide → 1-[5-Fluoro-2-(2,2,2-trifluoroethoxy)phenyl]piperazine

HRID 1840289노트

반응식

HRID 1840289 반응식
[F:1][C:2]1[CH:3]=[CH:4][C:5]([O:9][CH2:10][C:11]([F:14])([F:13])[F:12])=[C:6]([CH:8]=1)[NH2:7].Cl.Cl[CH2:17][CH2:18][NH:19][CH2:20][CH2:21]Cl.[I-].[K+].C(=O)([O-])[O-].[K+].[K+]>C(O)CCC>[F:1][C:2]1[CH:3]=[CH:4][C:5]([O:9][CH2:10][C:11]([F:12])([F:13])[F:14])=[C:6]([N:7]2[CH2:21][CH2:20][NH:19][CH2:18][CH2:17]2)[CH:8]=1

참가 물질

6

실험 절차

A stirred mixture of 0.52 g of Compound 5B, 0.45 g of bis-(2-chloroethyl)amine hydrochloride, 0.5 g of potassium iodide, 0.34 g of anhydrous potassium carbonate and 20 mL of n-butanol was refluxed for 32 hours under nitrogen. The solvent was removed under reduced pressure. The residue was treated with 10 mL of water and 10 mL of 20% aqueous sodium carbonate and extracted with 2×30 mL of ethyl acetate. The organic layer was washed with brine, dried over sodium sulphate and evaporated to dryness in vacuo. The residue was purified by flash chromatography (chloroform:2N ammonia in methanol gradient from 100:3 to 100:5) to afford 0.1 g (14%) of Compound 5C as an oil.

후처리

  1. temperaturewas refluxed for 32 hours under nitrogen
  2. customThe solvent was removed under reduced pressure
  3. additionThe residue was treated with 10 mL of water and 10 mL of 20% aqueous sodium carbonate
  4. extractionextracted with 2×30 mL of ethyl acetate
  5. washThe organic layer was washed with brine
  6. dry with materialdried over sodium sulphate
  7. customevaporated to dryness in vacuo
  8. customThe residue was purified by flash chromatography (chloroform:2N ammonia in methanol gradient from 100:3 to 100:5)

출처 및 근거

ORD 기록
ord-0f8a78bd7dd34fb88bd05ffb06ded490
출처 데이터셋
uspto-grants-2004_01
특허 번호
US06680319B2

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