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Hydrochloric Acid → 6-Bromo-3-(3-chlorophenyl)-4-hydroxyquinolin-2(1H)-one

HRID 627541
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HRID 627541 반응식
[Li]CCCC.C[Si](C)(C)N[Si](C)(C)C.[Br:15][C:16]1[CH:17]=[CH:18][C:19]([NH:26][C:27](=[O:36])[CH2:28][C:29]2[CH:34]=[CH:33][CH:32]=[C:31]([Cl:35])[CH:30]=2)=[C:20]([CH:25]=1)[C:21]([O:23]C)=O.Cl>C1COCC1>[Br:15][C:16]1[CH:25]=[C:20]2[C:19](=[CH:18][CH:17]=1)[NH:26][C:27](=[O:36])[C:28]([C:29]1[CH:34]=[CH:33][CH:32]=[C:31]([Cl:35])[CH:30]=1)=[C:21]2[OH:23]
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 4

HCID 313Hydrochloric AcidHCID 13838HexamethyldisilazaneHCID 86716102Methyl 5-bromo-2-(2-(3-chlorophenyl)acetamido)benzoateHCID 178418339Butyllithium

생성물 1

HCID 867161036-Bromo-3-(3-chlorophenyl)-4-hydroxyquinolin-2(1H)-one

시약·촉매·용매 1

HCID 8028Tetrahydrofuran
용매
2회

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온도
-40 °C

실험 절차

n-BuLi (1.6 M in hexane, 79 mL, 126 mmol) was added dropwise to a mixture of hexamethyldisilazane (26.7 mL, 126 mmol) in THF (150 mL) at −78° C. under nitrogen. The mixture was stirred for 1 hour, then was warmed to −40° C. A solution of methyl 5-bromo-2-(2-(3-chlorophenyl)acetamido)benzoate (21.1 g, 55 mmol, Intermediate 60, step a) in THF (150 mL) was added. The mixture was allowed to warm to room temperature and ice was added. The aqueous phase was acidified with 6 N aqueous HCl. The precipitate was collected by filtration, washed with DCM, and air-dried to yield the title compound.

후처리

  1. temperatureto warm to room temperature
  2. additionice was added
  3. filtrationThe precipitate was collected by filtration
  4. washwashed with DCM
  5. customair-dried

출처 및 근거

ORD 기록
ord-e1d7c9a46ee6426ca096bf869f061746
출처 데이터셋
uspto-grants-2016_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09309222B2

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