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2-Amino-5-chloro-3-fluoro-N-methoxy-N-methyl-benzamide → (2-Amino-5-chloro-3-fluoro-phenyl)-phenyl-methanone

HRID 1497229
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HRID 1497229 반응식
[NH2:1][C:2]1[C:13]([F:14])=[CH:12][C:11]([Cl:15])=[CH:10][C:3]=1[C:4](N(OC)C)=[O:5].[C:16]1([Mg]Br)[CH:21]=[CH:20][CH:19]=[CH:18][CH:17]=1>C(OCC)C>[NH2:1][C:2]1[C:13]([F:14])=[CH:12][C:11]([Cl:15])=[CH:10][C:3]=1[C:4]([C:16]1[CH:21]=[CH:20][CH:19]=[CH:18][CH:17]=1)=[O:5]
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참가 물질

4

반응물 2

HCID 866830482-Amino-5-chloro-3-fluoro-N-methoxy-N-methyl-benzamideHCID 178418255HCID 178418255, 화합물

생성물 1

HCID 86683049(2-Amino-5-chloro-3-fluoro-phenyl)-phenyl-methanone수율 70.7%

시약·촉매·용매 1

HCID 3283Diethyl Ether용매

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온도
0 °C

실험 절차

To a solution of 2-amino-5-chloro-3-fluoro-N-methoxy-N-methyl-benzamide (250 mg, 1.07 mmol) in diethyl ether (5 ml) was added phenylmagnesium bromide (2.69 ml, 1M in THF, 2.69 mmol) dropwise at 0° C. The resulting mixture was stirred for 2.5 h at 0° C. and the quenched by addition of saturated NH4Cl solution. The mixture was extracted with EtOAc and the combined organic extracts were washed with brine, dried with Na2SO4 and evaporated. The remaining residue was purified by column chromatography (silica gel, heptane/EtOAc 98:2-95:5) to afford the title compound (189 mg, 70%) as yellow solid. MS (ESI): 250.2 (M+H)+.

후처리

  1. customthe quenched by addition of saturated NH4Cl solution
  2. extractionThe mixture was extracted with EtOAc
  3. washthe combined organic extracts were washed with brine
  4. dry with materialdried with Na2SO4
  5. customevaporated
  6. customThe remaining residue was purified by column chromatography (silica gel, heptane/EtOAc 98:2-95:5)

출처 및 근거

ORD 기록
ord-b79081a81cd94b548b6c2fd895c68d76
출처 데이터셋
uspto-grants-2015_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09199938B2

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