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Ammonium Chloride → 6-Bromo-5-fluoro-1-N-methylbenzene-1,2-diamine

HRID 243186
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HRID 243186 반응식
[Cl-].[NH4+:2].[Br:3][C:4]1[C:9]([F:10])=[CH:8][CH:7]=[C:6]([N+:11]([O-])=O)[C:5]=1CN.[CH3:16]O.O>[Fe]>[Br:3][C:4]1[C:9]([F:10])=[CH:8][CH:7]=[C:6]([NH2:11])[C:5]=1[NH:2][CH3:16]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 25517Ammonium ChlorideHCID 22242641Methanol--water (1/1)HCID 68157229(2-Bromo-3-fluoro-6-nitrophenyl)methylamine

생성물 1

HCID 681576336-Bromo-5-fluoro-1-N-methylbenzene-1,2-diamine수율 47%

시약·촉매·용매 1

HCID 23925Iron촉매

실험 절차

Ammonium chloride (6.24 g, 117 mmol) and iron powder (4.34 g, 77.7 mmol) were added to a stirred mixture of (2-bromo-3-fluoro-6-nitrophenyl)methylamine (4.84 g, 19.4 mmol) in 3:1 methanol/water (320 mL) and the resultant mixture heated at reflux for 24 h. The solid material was removed by filtration and the filtrate concentrated to approximately ⅓ volume. This mixture was partitioned between DCM (3×) and water then the combined DCM extracts were dried (Na2SO4) and concentrated in vacuo. The resulting residue was purified by chromatography (SiO2, eluting with 0-5% methanol in DCM) to give title compound as an oil (1.99 g, 47%). LCMS (Method C): RT 2.37 min [M+H]+ 219.0, 221.0

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후처리

  1. temperatureat reflux for 24 h
  2. customThe solid material was removed by filtration
  3. concentrationthe filtrate concentrated to approximately ⅓ volume
  4. customThis mixture was partitioned between DCM (3×) and water
  5. dry with materialthe combined DCM extracts were dried (Na2SO4)
  6. concentrationconcentrated in vacuo
  7. customThe resulting residue was purified by chromatography (SiO2, eluting with 0-5% methanol in DCM)

출처 및 근거

ORD 기록
ord-2e22d1031c464714a8dc7005bfdf5c9e
출처 데이터셋
uspto-grants-2014_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08653089B2

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