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HCID 57355799、化合物 → Phthalimide

HRID 481035
ノート
印刷プレビュー

反応式

HRID 481035 の反応式
[N-]=C=S.N1CCC(N2C3C=CC=CC=3N(CCC[N:22]3[C:26](=[O:27])[C:25]4=[CH:28][CH:29]=[CH:30][CH:31]=[C:24]4[C:23]3=[O:32])C2=O)CC1>C(Cl)Cl.O>[C:26]1(=[O:27])[NH:22][C:23](=[O:32])[C:24]2=[CH:31][CH:30]=[CH:29][CH:28]=[C:25]12
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 57355799HCID 57355799、化合物HCID 178418790HCID 178418790、化合物

生成物 1

HCID 6809Phthalimide

試薬・触媒・溶媒 2

HCID 962Water溶媒HCID 6344Dichloromethane溶媒

実験手順

Di(2-pyridyl)thionocarbonate (0.286 g, 1.2 mM) was added to a cold (0° C.) solution of 1,1-di(p-anisyl)methyl amine (0.3 g, 1.2 mM) and triethylamine (0.17 ml) in methylene chloride (10 ml). The resulting mixture was slowly warmed up to RT over a 4 hour period then stirred at RT for additional 1 hour to provide the 1,1-di(p-anisyl)methyl isothiocyanate. The prepared isothiocyanate was added to Compound 53 (0.94 g, 0.43 mM), prepared in Example 53, dissolved in methylene chloride (10 ml). The mixture was stirred at RT overnight, diluted with water (20 ml) and the layers were separated. The aqueous layer was again extracted with methylene chloride (2×20 ml). The combined CH2Cl2 extracts were dried over MgSO4, evaporated in vacuo and chromatoraphed (EM silica gel 60, 10% EtOAc in CH2Cl2) to give the pthalimide intermediate. This intermediate, substituted for Compound 54, was treated as described in Example 55 to give the HCl salt of the product. m/z (MH+) 560

後処理

  1. customprepared in Example 53
  2. customthe layers were separated
  3. extractionThe aqueous layer was again extracted with methylene chloride (2×20 ml)
  4. dry with materialThe combined CH2Cl2 extracts were dried over MgSO4
  5. customevaporated in vacuo

出典と根拠

ORDレコード
ord-0a070f92f1e54b2092c17ab56acf1be1
出典データセット
uspto-grants-2003_11
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US06653478B2

反応ノート

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