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4-Bromoaniline → 2-(5-Bromo-pyridin-2-yl)-5-chloro-pentanoic acid (4-bromo-phenyl)-amide

HRID 220178
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HRID 220178 반응식
[Br:1][C:2]1[CH:3]=[CH:4][C:5]([CH:8]([CH2:12][CH2:13][CH2:14][Cl:15])[C:9]([OH:11])=O)=[N:6][CH:7]=1.CCN(CC)CC.C1CN([P+](Br)(N2CCCC2)N2CCCC2)CC1.F[P-](F)(F)(F)(F)F.[Br:47][C:48]1[CH:53]=[CH:52][C:51]([NH2:54])=[CH:50][CH:49]=1>C(Cl)Cl>[Br:47][C:48]1[CH:53]=[CH:52][C:51]([NH:54][C:9](=[O:11])[CH:8]([C:5]2[CH:4]=[CH:3][C:2]([Br:1])=[CH:7][N:6]=2)[CH2:12][CH2:13][CH2:14][Cl:15])=[CH:50][CH:49]=1
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참가 물질

6

반응물 4

HCID 78074-BromoanilineHCID 8471TriethylamineHCID 2733179PyBroPHCID 592382662-(5-Bromo-pyridin-2-yl)-5-chloro-pentanoic acid

생성물 1

HCID 592382942-(5-Bromo-pyridin-2-yl)-5-chloro-pentanoic acid (4-bromo-phenyl)-amide

시약·촉매·용매 1

HCID 6344Dichloromethane
용매

실험 절차

To a solution of 2-(5-Bromo-pyridin-2-yl)-5-chloro-pentanoic acid (1.9 g, 6.5 mmol), Et3N (3.6 mL, 26 mmol), and Pybrop (6 g, 13 mmol) in CH2Cl2 (30 mL) was added 4-bromo-phenylamine (1.45 g, 8.45 mmol). This mixture was stirred overnight at room temperature and then evaporated. The mixture was redissolved in EtOAc (40 mL) and washed with 2N HCl (20 mL×3), brine, 5% NaHCO3 (20 mL×3), brine, dried with Na2SO4, filtered and evaporated. The residue was purified by column chromatography on silica gel using hexane/EtOAc to give a white solid (1.63 g, 56% for two steps). MS: calc'd 444 (MH+), exp 444 (MH+). 1H NMR (400 MHz, CDCl3-d) 9.65 (broad s, 1H), 8.72 (d, 1H, J=2.0 Hz), 8.06 (d, 1H, J=8.4 Hz), 7.53-7.41 (m, 4H), 4.18-4.08 (m, 1H), 3.66-3.54 (m, 2H), 2.45-2.35 (m, 1H), 2.21-2.11 (m, 1H), 1.98-1.87 (m, 1H), 1.83-1.72 (m, 1H).

후처리

  1. customevaporated
  2. dissolutionThe mixture was redissolved in EtOAc (40 mL)
  3. washwashed with 2N HCl (20 mL×3), brine, 5% NaHCO3 (20 mL×3), brine
  4. dry with materialdried with Na2SO4
  5. filtrationfiltered
  6. customevaporated
  7. customThe residue was purified by column chromatography on silica gel
  8. customto give a white solid (1.63 g, 56% for two steps)

출처 및 근거

ORD 기록
ord-37abab0d833d4ed6b72a3cd9ac56a8c5
출처 데이터셋
uspto-grants-2012_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08202866B2

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