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Acetic Acid → Tert-butyl 4-(4-amino-3-fluorophenyl)piperazine-1-carboxylate

HRID 1503838
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HRID 1503838 반응식
[F:1][C:2]1[CH:3]=[C:4]([N:11]2[CH2:16][CH2:15][N:14]([C:17]([O:19][C:20]([CH3:23])([CH3:22])[CH3:21])=[O:18])[CH2:13][CH2:12]2)[CH:5]=[CH:6][C:7]=1[N+:8]([O-])=O.C(O)(=O)C>[Zn].O1CCCC1.CO>[NH2:8][C:7]1[CH:6]=[CH:5][C:4]([N:11]2[CH2:16][CH2:15][N:14]([C:17]([O:19][C:20]([CH3:22])([CH3:21])[CH3:23])=[O:18])[CH2:13][CH2:12]2)=[CH:3][C:2]=1[F:1]
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참가 물질

5

반응물 2

HCID 176Acetic AcidHCID 66738172Tert-butyl 4-(3-fluoro-4-nitrophenyl)piperazine-1-carboxylate

생성물 1

HCID 57652076Tert-butyl 4-(4-amino-3-fluorophenyl)piperazine-1-carboxylate

시약·촉매·용매 2

HCID 23994Zinc촉매HCID 21899815MeOH tetrahydrofuran용매

실험 절차

A mixture of the product of Example 28A (1.6 g, 4.9 mmol), zinc dust (3.2 g, 49 mmol) and acetic acid (5.4 mL) in 1/1 tetrahydrofuran/methanol (100 mL) was stirred at ambient temperature for 1 hour. The mixture was filtered and the filtrate was diluted with water and adjusted to pH 9. The mixture was extracted with ethyl acetate and the combined organic phase was washed with brine, dried over sodium sulfate, filtered and concentrated. The residue was purified by flash chromatography on silica gel (200-300 mesh) eluting with 99/1 dichloromethane/methanol to give the title compound. MS: 296 (M+H+).

후처리

  1. filtrationThe mixture was filtered
  2. additionthe filtrate was diluted with water
  3. extractionThe mixture was extracted with ethyl acetate
  4. washthe combined organic phase was washed with brine
  5. dry with materialdried over sodium sulfate
  6. filtrationfiltered
  7. concentrationconcentrated
  8. customThe residue was purified by flash chromatography on silica gel (200-300 mesh)
  9. washeluting with 99/1 dichloromethane/methanol

출처 및 근거

ORD 기록
ord-f86f30308d844574881c63cbdf09ac61
출처 데이터셋
uspto-grants-2015_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09212192B2

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