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Water → 6-Bromo-4-hydroxy-3-phenoxyquinolin-2(1H)-one

HRID 520840
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HRID 520840 반응식
[Br:1][C:2]1[CH:3]=[CH:4][C:5]([NH:12][C:13](=[O:22])[CH2:14][O:15][C:16]2[CH:21]=[CH:20][CH:19]=[CH:18][CH:17]=2)=[C:6]([CH:11]=1)[C:7](OC)=[O:8].C[Si]([N-][Si](C)(C)C)(C)C.[K+].O>O1CCCC1>[Br:1][C:2]1[CH:11]=[C:6]2[C:5](=[CH:4][CH:3]=1)[NH:12][C:13](=[O:22])[C:14]([O:15][C:16]1[CH:21]=[CH:20][CH:19]=[CH:18][CH:17]=1)=[C:7]2[OH:8]
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참가 물질

5

반응물 3

HCID 962WaterHCID 3251421Potassium bis(trimethylsilyl)amideHCID 7765744Methyl 5-bromo-2-(2-phenoxyacetamido)benzoate

생성물 1

HCID 867154446-Bromo-4-hydroxy-3-phenoxyquinolin-2(1H)-one

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매

반응 조건

온도
0 °C

실험 절차

To a solution of methyl 5-bromo-2-(2-phenoxyacetamido)benzoate (7.28 g, 20.0 mmol, Intermediate 5: step a) in tetrahydrofuran (215 mL) at −78° C. was added potassium bis(trimethylsilyl)amide (0.5 M solution in toluene, 118.7 mL, 59.37 mmol) over 7 minutes. The mixture was stirred at −78° C. for 5 minutes and 0° C. for 1.5 hours. The resulting cold solution was quenched with water. The white solid formed was completely dissolved by addition of excess water. The aqueous phase was washed once with EtOAc and then acidified by slow addition of 2 N aqueous HCl solution (kept pH above 2). The off-white precipitate formed was filtered and dried in the air overnight and at 40° C. for 1 hour to provide the title compound.

후처리

  1. customThe resulting cold solution was quenched with water
  2. customThe white solid formed
  3. washThe aqueous phase was washed once with EtOAc
  4. additionacidified by slow addition of 2 N aqueous HCl solution (kept pH above 2)
  5. customThe off-white precipitate formed
  6. filtrationwas filtered
  7. customdried in the air overnight and at 40° C. for 1 hour

출처 및 근거

ORD 기록
ord-c8032877c4bc4c1995aa4c6690107a70
출처 데이터셋
uspto-grants-2016_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09328095B2

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