(+-)-1-Aminoindan → N1-(2,3-Dihydro-1H-indenyl)-N4-(1H-5-indazolyl)-1,4-cyclohexanediamine

HRID 1352160

反応式

HRID 1352160 の反応式
[NH:1]1[C:9]2[C:4](=[CH:5][C:6]([NH:10][CH:11]3[CH2:16][CH2:15][C:14](=O)[CH2:13][CH2:12]3)=[CH:7][CH:8]=2)[CH:3]=[N:2]1.[NH2:18][CH:19]1[C:27]2[C:22](=[CH:23][CH:24]=[CH:25][CH:26]=2)[CH2:21][CH2:20]1.C(O[BH-](OC(=O)C)OC(=O)C)(=O)C.[Na+].Cl.CO>CO>[CH:19]1([NH:18][CH:14]2[CH2:15][CH2:16][CH:11]([NH:10][C:6]3[CH:5]=[C:4]4[C:9](=[CH:8][CH:7]=3)[NH:1][N:2]=[CH:3]4)[CH2:12][CH2:13]2)[C:27]2[C:22](=[CH:23][CH:24]=[CH:25][CH:26]=2)[CH2:21][CH2:20]1

参加物

6

反応物 4

HCID 123445(+-)-1-AminoindanHCID 5049666Sodium triacetoxyborohydrideHCID 178382714-(1H-5-Indazolylamino)-1-cyclohexanone2 回HCID 21893726Hydrochloride methanol

生成物 1

HCID 17838257N1-(2,3-Dihydro-1H-indenyl)-N4-(1H-5-indazolyl)-1,4-cyclohexanediamine収率 19.7%

試薬・触媒・溶媒 1

HCID 887Methanol溶媒

実験手順

4-(1H-5-Indazolylamino)-1-cyclohexanone (intermediate 3) (57 mg) and 1-aminoindan (67 mg) were dissolved in methanol (1 ml), and sodium triacetoxyborohydride (105 mg) was added by portions to the solution at room temperature. The reaction mixture was stirred at room temperature for 18 hr. Hydrochloric acid-methanol was then added thereto, and the reaction mixture was stirred and was then concentrated. The residue was purified by HPLC [0.5% aqueous trifluoroacetic acid solution/acetonitrile]. A saturated aqueous sodium hydrogencarbonate solution (2 ml) was then added to fractions containing respective compounds, followed by extraction with chloroform-propanol (3/1). The organic layers were dried over anhydrous sodium sulfate, and the solvent was removed by distillation under the reduced pressure to give an anti-form compound (17 mg) and a syn-form compound (18 mg).

後処理

  1. stirringthe reaction mixture was stirred
  2. concentrationwas then concentrated
  3. customThe residue was purified by HPLC [0.5% aqueous trifluoroacetic acid solution/acetonitrile]
  4. additionA saturated aqueous sodium hydrogencarbonate solution (2 ml) was then added to fractions
  5. additioncontaining respective compounds
  6. extractionfollowed by extraction with chloroform-propanol (3/1)
  7. dry with materialThe organic layers were dried over anhydrous sodium sulfate
  8. customthe solvent was removed by distillation under the reduced pressure

出典と根拠

ORDレコード
ord-93cf0d96e2fe4c92b0e0eea90875b832
出典データセット
uspto-grants-2007_05
特許番号
US07217722B2

関連ノート

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