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Ammonium Acetate → 2-Amino-4-bromo-5-iodo-3-methoxy-6-methylbenzamide

HRID 17293
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HRID 17293 반응식
[Br:1][C:2]1[CH:13]=[C:6]2[NH:7]C(=O)O[C:10](=[O:11])[CH:5]2[C:4](OC)([CH3:14])[C:3]=1[I:17].[C:18]([O-:21])(=O)C.[NH4+:22]>CN(C)C=O>[NH2:7][C:6]1[C:13]([O:21][CH3:18])=[C:2]([Br:1])[C:3]([I:17])=[C:4]([CH3:14])[C:5]=1[C:10]([NH2:22])=[O:11]
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참가 물질

4

반응물 2

HCID 517165Ammonium AcetateHCID 866308087-bromo-6-iodo-5-methoxy-5-methyl-1H-benzo[d][1,3]oxazine-2,4-dione

생성물 1

HCID 860974252-Amino-4-bromo-5-iodo-3-methoxy-6-methylbenzamide수율 50.3%

시약·촉매·용매 1

HCID 6228Dimethylformamide용매

실험 절차

Under nitrogen atmosphere, 7-bromo-6-iodo-5-methoxy-5-methyl-1H-benzo[d][1,3]oxazine-2,4-dione (I-32) (3.68 g, 8.93 mmol) and ammonium acetate (3.44 g, 44.7 mmol) were added to dewatered N,N-dimethylformamide (80 ml), followed by stirring at room temperature for 2 hours. The reaction liquid was concentrated under reduced pressure, ethyl acetate and water were added to the residue, the precipitated insoluble matter was separated by filtration. The organic layer was collected by liquid-liquid separation, washed with aqueous saturated sodium chloride solution and dried on anhydrous magnesium sulfate, the solvent was evaporated away under reduced pressure to obtain the entitled compound (1.73 g, 50%) as a brown solid. Not further purified, this was used in the next reaction.

후처리

  1. customThe reaction liquid
  2. concentrationwas concentrated under reduced pressure, ethyl acetate and water
  3. additionwere added to the residue
  4. customthe precipitated insoluble matter was separated by filtration
  5. customThe organic layer was collected by liquid-liquid separation
  6. washwashed with aqueous saturated sodium chloride solution
  7. dry with materialdried on anhydrous magnesium sulfate
  8. customthe solvent was evaporated away under reduced pressure

출처 및 근거

ORD 기록
ord-a215b62a0d274023a603552ce10a7081
출처 데이터셋
uspto-grants-2010_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07737166B2

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