Water → 3-(2-Aminoethyl)-7-nitro-1,2,4,5-tetrahydro-3H-3-benzazepine

HRID 329373ノート

反応式

HRID 329373 の反応式
C1(P(C2C=CC=CC=2)C2C=CC=CC=2)C=CC=CC=1.[N:20]([CH2:23][CH2:24][N:25]1[CH2:31][CH2:30][C:29]2[CH:32]=[CH:33][C:34]([N+:36]([O-:38])=[O:37])=[CH:35][C:28]=2[CH2:27][CH2:26]1)=[N+]=[N-].O>O1CCCC1>[NH2:20][CH2:23][CH2:24][N:25]1[CH2:31][CH2:30][C:29]2[CH:32]=[CH:33][C:34]([N+:36]([O-:38])=[O:37])=[CH:35][C:28]=2[CH2:27][CH2:26]1

参加物

5

実験手順

Triphenylphosphine (0.71 g) was added to a solution of 3-(2-azidoethyl)-7-nitro-1,2,4,5-tetrahydro-3H-3-benzazepine (0.68 g) in dry tetrahydrofuran under a nitrogen atmosphere and the reaction mixture was then stirred at room temperature for 18 hours and heated at 50° for 5 hours. After cooling, water was added and the mixture was stirred at room temperature for 3 days. The solvent was then evaporated in vacuo and the residue was diluted with 2M hydrochloric acid and washed three times with ethyl acetate. The aqueous layer was made alkaline (pH=12) with 5M sodium hydroxide and extracted three times with ethyl acetate. The latter organic extracts were combined and dried (Na2SO4), filtered and evaporated in vacuo to give the title compound as an oil, yield 0.56 g, which was used without further purification.

後処理

  1. temperatureheated at 50° for 5 hours
  2. temperatureAfter cooling
  3. stirringthe mixture was stirred at room temperature for 3 days
  4. customThe solvent was then evaporated in vacuo
  5. additionthe residue was diluted with 2M hydrochloric acid
  6. washwashed three times with ethyl acetate
  7. extractionextracted three times with ethyl acetate
  8. dry with materialdried (Na2SO4)
  9. filtrationfiltered
  10. customevaporated in vacuo

出典と根拠

ORDレコード
ord-12844719546c44c1a697218e673769bc
出典データセット
uspto-grants-1990_01
特許番号
US04891372

反応ノート

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