Diisopropylethylamine → methyl 4-(4-nitro-2,3-dihydro-1H-inden-1-yl)piperazine-1-carboxylate

HRID 2237419ノート

反応式

HRID 2237419 の反応式
Cl[CH:2]1[C:10]2[C:5](=[C:6]([N+:11]([O-:13])=[O:12])[CH:7]=[CH:8][CH:9]=2)[CH2:4][CH2:3]1.CCN(C(C)C)C(C)C.Cl.[CH3:24][O:25][C:26]([N:28]1[CH2:33][CH2:32][NH:31][CH2:30][CH2:29]1)=[O:27]>C(#N)C.CCOC(C)=O>[N+:11]([C:6]1[CH:7]=[CH:8][CH:9]=[C:10]2[C:5]=1[CH2:4][CH2:3][CH:2]2[N:31]1[CH2:32][CH2:33][N:28]([C:26]([O:25][CH3:24])=[O:27])[CH2:29][CH2:30]1)([O-:13])=[O:12]

参加物

6

反応条件

温度
79 °C

実験手順

To a room temperature solution of 1-Chloro-4-nitro-2,3-dihydro-1H-indene (221 mg, 1.12 mmol, 1.0 equiv) and DIPEA (430 μL, 2.46 mmol, 2.2 equiv) in dry acetonitrile (1.6 mL) was added methylpiperazine carboxylate hydrochloride salt (444 mg, 2.46 mmol, 2.2 equiv) as a solid in one portion. The resulting reaction mixture was heated to 79° C. overnight. The reaction mixture was allowed to cool to RT and diluted with EtOAc. The organic layer was extracted with 1 M HCl (3×20 mL), and the combined aqueous layers were treated with 3 N NaOH until the pH=10. The resulting solution was extracted three times with EtOAc, and the combined organic layers were dried over sodium sulfate, filtered and concentrated in vacuo to provide the title compound as a brown oil (239 mg, 78%). LCMS [M+H]+=306.1.

後処理

  1. customThe resulting reaction mixture
  2. temperatureto cool to RT
  3. extractionThe organic layer was extracted with 1 M HCl (3×20 mL)
  4. additionthe combined aqueous layers were treated with 3 N NaOH until the pH=10
  5. extractionThe resulting solution was extracted three times with EtOAc
  6. dry with materialthe combined organic layers were dried over sodium sulfate
  7. filtrationfiltered
  8. concentrationconcentrated in vacuo

出典と根拠

ORDレコード
ord-a2a4f8fa6a8249c5aaf2e8ca1e07fd16
出典データセット
uspto-grants-2010_05
特許番号
US07718657B2

反応ノート

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