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Hydrazine → Pyrrolo(1,2-a)(1,4)diazepine

HRID 439982
ノート
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反応式

HRID 439982 の反応式
[N+](C1C=CC(C([N:10]2[C:16]3OC=C[C:15]=3[CH2:14][N:13]3[CH:20]=[CH:21][CH:22]=[C:12]3[CH2:11]2)=O)=CC=1)([O-])=O.NN>C(O)C.[Pd]>[CH:11]1[C:12]2[N:13]([CH:20]=[CH:21][CH:22]=2)[CH2:14][CH:15]=[CH:16][N:10]=1
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 2

HCID 9321HydrazineHCID 218370989,10-dihydro-10-(4-nitrobenzoyl)-4H-furo[2,3-e]pyrrolo[1,2-a][1,4]diazepine

生成物 1

HCID 45087533Pyrrolo(1,2-a)(1,4)diazepine

試薬・触媒・溶媒 2

HCID 23938Palladium触媒HCID 702Ethanol溶媒

実験手順

To a solution of i mmol of 9,10-dihydro-10-(4-nitrobenzoyl)-4H-furo[2,3-e]pyrrolo[1,2-a][1,4]-diazepine in 20 ml of ethyl alcohol is added 0.2 g of 10% Pd/C and 2.5 mmol of hydrazine followed by stirring and heating under reflux for 3 hours. The room temperature reaction mixture is filtered through diatomaceous earth and the filtrate concentrated in vacuo. The residue is dissolved in methylene chloride and passed through a thin pad of hydrous magnesium silicate. The filtrate is concentrated in vacuo to give the desired product which is purified by flash chromatography on silica gel to give the desired product as a solid.

このページの内容参加物実験手順後処理出典と根拠反応ノート

後処理

  1. temperatureheating
  2. temperatureunder reflux for 3 hours
  3. customThe room temperature reaction mixture
  4. filtrationis filtered through diatomaceous earth
  5. concentrationthe filtrate concentrated in vacuo
  6. dissolutionThe residue is dissolved in methylene chloride
  7. concentrationThe filtrate is concentrated in vacuo

出典と根拠

ORDレコード
ord-4f303ab7db724eb395e74822a1956802
出典データセット
uspto-grants-1996_05
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05516774

反応ノート

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