Methyl chloroformate → 1-(N-benzyl-tert.-butylamino)-3-(2-hydroxy-3-methoxycarbonylamino-phenoxy)-2-propanol

HRID 1391052ノート

反応式

HRID 1391052 の反応式
[CH2:1]([N:8]([C:22]([CH3:25])([CH3:24])[CH3:23])[CH2:9][CH:10]([OH:21])[CH2:11][O:12][C:13]1[CH:18]=[CH:17][CH:16]=[C:15]([NH2:19])[C:14]=1[OH:20])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.Cl[C:27]([O:29][CH3:30])=[O:28]>C(O)(C)C.O>[CH2:1]([N:8]([C:22]([CH3:25])([CH3:24])[CH3:23])[CH2:9][CH:10]([OH:21])[CH2:11][O:12][C:13]1[CH:18]=[CH:17][CH:16]=[C:15]([NH:19][C:27]([O:29][CH3:30])=[O:28])[C:14]=1[OH:20])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1

参加物

4

実験手順

14.5 g of 1-(N-benzyl-tert.-butylamino)-3-(3-amino-2-hydroxy-phenoxy)-2-propanol are dissolved in 140 ml of an isopropanol/water mixture (1:1) and 5.0 ml of methyl chloroformate are added, at 15°-20°, whilst stirring vigorously and stirring is continued for a further 11/2 hours at room temperature, the reaction mixture is then evaporated and the residue is dissolved in 50 ml of water. After extraction with 20 ml of ethyl acetate, the acid aqueous phase is rendered alkaline with concentrated sodium hydroxide solution and extracted with 3 times 100 ml of methylene chloride. Evaporation of the organic phase gives the crude base, from which crystalline 1-(N-benzyl-tert.-butylamino)-3-(2-hydroxy-3-methoxycarbonylamino-phenoxy)-2-propanol with a melting point of 130°-133° is isolated.

後処理

  1. stirringstirring
  2. custom2 hours
  3. customat room temperature
  4. customthe reaction mixture is then evaporated
  5. dissolutionthe residue is dissolved in 50 ml of water
  6. extractionAfter extraction with 20 ml of ethyl acetate
  7. extractionextracted with 3 times 100 ml of methylene chloride
  8. customEvaporation of the organic phase
  9. customgives the crude base

出典と根拠

ORDレコード
ord-bfbc954991d94e99ade9f81a699dc2fe
出典データセット
uspto-grants-1979_02
特許番号
US04140789

反応ノート

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