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Trifluoromethanesulfonic anhydride → Trifluoromethanesulfonic acid 7-chloro-3-(3,5-dimethylphenyl)-6-nitro-2-oxo-1,2-dihydroquinolin-4-yl ester

HRID 1857638
ノート
印刷プレビュー

反応式

HRID 1857638 の反応式
C1(C2CCCCCCCCCC=2)CCCCCCCCNN=1.[F:23][C:24]([F:37])([F:36])[S:25]([O:28]S(C(F)(F)F)(=O)=O)(=[O:27])=[O:26].[Cl:38][C:39]1[CH:48]=[C:47]2[C:42]([C:43](O)=[C:44]([C:50]3[CH:55]=[C:54]([CH3:56])[CH:53]=[C:52]([CH3:57])[CH:51]=3)[C:45](=[O:49])[NH:46]2)=[CH:41][C:40]=1[N+:59]([O-:61])=[O:60]>>[Cl:38][C:39]1[CH:48]=[C:47]2[C:42]([C:43]([O:28][S:25]([C:24]([F:37])([F:36])[F:23])(=[O:27])=[O:26])=[C:44]([C:50]3[CH:55]=[C:54]([CH3:56])[CH:53]=[C:52]([CH3:57])[CH:51]=3)[C:45](=[O:49])[NH:46]2)=[CH:41][C:40]=1[N+:59]([O-:61])=[O:60]
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 3

HCID 67749Trifluoromethanesulfonic anhydrideHCID 536302743-(Cycloundecen-1-yl)-1,2-diazacycloundec-2-eneHCID 547112387-chloro-3-(3,5-dimethylphenyl)-4-hydroxy-6-nitro-1H-quinolin-2-one

生成物 1

HCID 54023713Trifluoromethanesulfonic acid 7-chloro-3-(3,5-dimethylphenyl)-6-nitro-2-oxo-1,2-dihydroquinolin-4-yl ester

反応条件

温度
-78 °C

実験手順

To a solution of 7-chloro-3-(3,5-dimethylphenyl)-4-hydroxy-6-nitro-1H-quinolin-2-one (1.0 g in 50 mL dry methylene chloride) was added 0.455 ml diazabicycloundecene and the mixture cooled to -78° C. To this was added trifluoromethanesulfonic anhydride (0.51 mL) dropwise via syringe and the mixture stirred at low temperature. After 1 hour, the reaction was quenched by the addition of saturated ammonium chloride (35 mL) and extracted with ethyl acetate (3×75 mL). The organics were washed with water (50 mL) and brine (50 mL) then dried over magnesium sulfate. Purification of the concentrate by flash chromatography on silica gel (hexane:ethyl acetate, 3:2) gave the title compound (629 mg).

後処理

  1. customthe reaction was quenched by the addition of saturated ammonium chloride (35 mL)
  2. extractionextracted with ethyl acetate (3×75 mL)
  3. washThe organics were washed with water (50 mL) and brine (50 mL)
  4. dry with materialthen dried over magnesium sulfate
  5. customPurification of the
  6. concentrationconcentrate by flash chromatography on silica gel (hexane:ethyl acetate, 3:2)

出典と根拠

ORDレコード
ord-59911d1c1743434daa7684f1673764f6
出典データセット
uspto-grants-2000_11
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US06147088

反応ノート

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