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Hydrochloric Acid → 6-(2,6-Dimethoxyphenyl)-1-(4-(trifluoromethoxy)benzyl)piperazine-2,5-dione

HRID 594411
ノート
印刷プレビュー

反応式

HRID 594411 の反応式
C([O:5][C:6]([NH:8][CH2:9][C:10]([N:12]([CH:25]([C:31]1[C:36]([O:37][CH3:38])=[CH:35][CH:34]=[CH:33][C:32]=1[O:39][CH3:40])C(OCC)=O)[CH2:13][C:14]1[CH:19]=[CH:18][C:17]([O:20][C:21]([F:24])([F:23])[F:22])=[CH:16][CH:15]=1)=[O:11])=O)(C)(C)C.Cl.O1CCOCC1>C(Cl)Cl>[CH3:38][O:37][C:36]1[CH:35]=[CH:34][CH:33]=[C:32]([O:39][CH3:40])[C:31]=1[CH:25]1[N:12]([CH2:13][C:14]2[CH:19]=[CH:18][C:17]([O:20][C:21]([F:23])([F:22])[F:24])=[CH:16][CH:15]=2)[C:10](=[O:11])[CH2:9][NH:8][C:6]1=[O:5]
参加物実験手順後処理出典と根拠反応ノート

参加物

5

反応物 3

HCID 313Hydrochloric AcidHCID 312751,4-DioxaneHCID 86695634ethyl 2-(2-((tert-butoxycarbonyl)amino)-N-(4-(trifluoromethoxy)benzyl)acetamido)-2-(2,6-dimethoxyphenyl)acetate

生成物 1

HCID 690802006-(2,6-Dimethoxyphenyl)-1-(4-(trifluoromethoxy)benzyl)piperazine-2,5-dione

試薬・触媒・溶媒 1

HCID 6344Dichloromethane溶媒

実験手順

A cooled (0° C.) solution of ethyl 2-(2-((tert-butoxycarbonyl)amino)-N-(4-(trifluoromethoxy)-benzyl)acetamido)-2-(2,6-dimethoxyphenyl)acetate (900 mg; 1.57 mmol) in anh. DCM (18 ml) was treated dropwise with 4 M HCl in dioxane (6.00 ml; 24.00 mmol), and the resulting mixture was further stirred at rt, under nitrogen, for 2.5 h. The reaction mixture was concentrated to dryness under reduced pressure, the resulting residue was treated with aq. sat. NaHCO3 (7.5 ml) and AcOEt (7.5 ml), and stirring at rt was then continued for 17 h. The separated aq. layer was extracted with AcOEt (20 ml), and the mixed organic layers were washed with brine, dried over anh. MgSO4, filtered, and concentrated to dryness under reduced pressure affording 6-(2,6-dimethoxyphenyl)-1-(4-(trifluoromethoxy)benzyl)-piperazine-2,5-dione as a slightly orange solid. LC-MS (conditions D): tR=0.94 min.; [M+H]+: 424.88 g/mol.

後処理

  1. concentrationThe reaction mixture was concentrated to dryness under reduced pressure
  2. additionthe resulting residue was treated with aq. sat. NaHCO3 (7.5 ml) and AcOEt (7.5 ml)
  3. stirringstirring at rt
  4. waitwas then continued for 17 h
  5. extractionThe separated aq. layer was extracted with AcOEt (20 ml)
  6. washthe mixed organic layers were washed with brine
  7. dry with materialdried over anh. MgSO4
  8. filtrationfiltered
  9. concentrationconcentrated to dryness under reduced pressure

出典と根拠

ORDレコード
ord-6ff7e32805c44790bd541ee7908e8be3
出典データセット
uspto-grants-2016_01
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US09242970B2

反応ノート

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