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Sodium ethoxide → 2-Amino-5-(2-naphthyl)pyrrole-3-carboxamide

HRID 416023
ノート
印刷プレビュー

反応式

HRID 416023 の反応式
[O-][CH2:2][CH3:3].[Na+].[CH2:5]([C:9]([NH2:11])=[O:10])[C:6]([NH2:8])=[NH:7].Cl.BrCC([C:17]1[C:26]2[C:21](=[CH:22][CH:23]=[CH:24][CH:25]=2)[CH:20]=[CH:19][CH:18]=1)=O>C(O)C>[NH2:7][C:6]1[NH:8][C:2]([C:19]2[CH:18]=[CH:17][C:26]3[C:21](=[CH:22][CH:23]=[CH:24][CH:25]=3)[CH:20]=2)=[CH:3][C:5]=1[C:9]([NH2:11])=[O:10]
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 2723922Sodium ethoxideHCID 3084595Amidinomalonamide hydrochlorideHCID 38305132-Bromo-1-(1-naphthalenyl)ethanone

生成物 1

HCID 582940172-Amino-5-(2-naphthyl)pyrrole-3-carboxamide収率 30%

試薬・触媒・溶媒 1

HCID 702Ethanol溶媒

実験手順

Under ice-cooling, sodium ethoxide (2.7 g, 40 mmol) was added to a suspension of malonamamidine hydrochloride (5.5 g, 40 mmol) in dehydrated ethanol (130 mL), and then the mixture was stirred for 20 minutes. 2-Bromoacetylnaphthalene (5.0 g, 20 mmol) was added thereto, and the whole was stirred at room temperature overnight. The reaction mixture was concentrated in vacuo, and the obtained residue was purified by silica gel column chromatography to give the title reference compound (1.5 g) as a black solid (Yield 30%).

後処理

  1. temperatureUnder ice-cooling
  2. stirringthe whole was stirred at room temperature overnight
  3. concentrationThe reaction mixture was concentrated in vacuo
  4. customthe obtained residue was purified by silica gel column chromatography

出典と根拠

ORDレコード
ord-47df18e4a63c4970aacb527f05a45fd8
出典データセット
uspto-grants-2012_01
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08088817B2

反応ノート

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