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Pyridine → N-(3-amino-2-methoxy-5-trifluoromethyl-phenyl)-methanesulfonamide

HRID 1179141
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HRID 1179141 반응식
[CH3:1][O:2][C:3]1[C:8]([NH2:9])=[CH:7][C:6]([C:10]([F:13])([F:12])[F:11])=[CH:5][C:4]=1[NH2:14].N1C=CC=CC=1.[CH3:21][S:22](Cl)(=[O:24])=[O:23].CCOC(C)=O>ClCCl>[NH2:9][C:8]1[C:3]([O:2][CH3:1])=[C:4]([NH:14][S:22]([CH3:21])(=[O:24])=[O:23])[CH:5]=[C:6]([C:10]([F:12])([F:11])[F:13])[CH:7]=1
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참가 물질

6

반응물 4

HCID 1049PyridineHCID 8857Ethyl AcetateHCID 31297Methanesulfonyl chloride2회HCID 225069942-Methoxy-5-(trifluoromethyl)benzene-1,3-diamine

생성물 1

HCID 22506980N-(3-amino-2-methoxy-5-trifluoromethyl-phenyl)-methanesulfonamide수율 58.2%

시약·촉매·용매 1

HCID 6344
Dichloromethane
용매

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온도
0 °C

실험 절차

2-Methoxy-5-trifluoromethylbenzene-1,3-diamine (2.32 g, 11.3 mmol) was dissolved in 50 mL anhydrous dichloromethane. The solution was cooled to 0° C., and pyridine (3.64 mL, 45.0 mmol) and methane sulfonyl chloride (0.89 mL, 11.5 mmol) were added. The reaction was left to stir overnight at room temperature. A few more drops (0.1 mL) of methane sulfonyl chloride were added and the reaction stirred an extra day. Then 200 mL EtOAc, was added and the solution washed once with 100 mL water, twice with 15 mL saturated aqueous NH4Cl solution and finally with brine. The organic solution was dried (MgSO4), filtered and concentrated in vacuo. The residue was purified by column chromatography on silica gel using EtOAc/hexanes eluent mixtures, providing N-(3-amino-2-methoxy-5-trifluoromethyl-phenyl)-methanesulfonamide (1870 mg, 6.58 mmol, 58% yield) as an orange solid.

후처리

  1. waitThe reaction was left
  2. stirringthe reaction stirred an extra day
  3. washthe solution washed once with 100 mL water, twice with 15 mL saturated aqueous NH4Cl solution and finally with brine
  4. dry with materialThe organic solution was dried (MgSO4)
  5. filtrationfiltered
  6. concentrationconcentrated in vacuo
  7. customThe residue was purified by column chromatography on silica gel

출처 및 근거

ORD 기록
ord-a7e142fc78ee47cbaa9d6d14f0e9f0b4
출처 데이터셋
uspto-grants-2007_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07279475B2

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