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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
ノート
印刷プレビュー

反応式

HRID 1497229 の反応式
[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]
参加物反応条件実験手順後処理出典と根拠反応ノート

参加物

4

反応物 2

HCID 866830482-Amino-5-chloro-3-fluoro-N-methoxy-N-methyl-benzamideHCID 178418255HCID 178418255、化合物

生成物 1

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

試薬・触媒・溶媒 1

HCID 3283Diethyl Ether溶媒

反応条件

温度
0 °C

実験手順

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)+.

後処理

  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)

出典と根拠

ORDレコード
ord-b79081a81cd94b548b6c2fd895c68d76
出典データセット
uspto-grants-2015_12
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US09199938B2

反応ノート

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