N-Hydroxyphthalimide → HCID 22861110, 화합물

HRID 439893노트

반응식

HRID 439893 반응식
N(C(OCC)=O)=NC(OCC)=O.[C:13]([NH:20][CH2:21][C@H:22]1[CH2:24][C@H:23]1[CH2:25][OH:26])([O:15][C:16]([CH3:19])([CH3:18])[CH3:17])=[O:14].O[N:28]1[C:32](=[O:33])[C:31]2=[CH:34][CH:35]=[CH:36][CH:37]=[C:30]2[C:29]1=[O:38].C1(P(C2C=CC=CC=2)C2C=CC=CC=2)C=CC=CC=1>C1C=CC=CC=1>[C:13]([NH:20][CH2:21][C@H:22]1[CH2:24][C@H:23]1[CH2:25][O:26][N:28]1[C:32](=[O:33])[C:31]2[C:30](=[CH:37][CH:36]=[CH:35][CH:34]=2)[C:29]1=[O:38])([O:15][C:16]([CH3:19])([CH3:18])[CH3:17])=[O:14]

참가 물질

6

실험 절차

A solution of 2.61 ml (0.0157 mol) of diethyl azodicarboxylate (93%) in 15 ml of benzene is added dropwise to a mixture of 3 g (0.0149 mol) of cis-2-(N-BOC-aminomethyl)-cyclopropanemethanol, 2.43 g (0.0149 mol) of N-hydroxyphthalimide, 3.9 g (0.0149 mol) of triphenylphosphine and 120 ml of benzene at 20°-30° C., while stirring. The reaction mixture is stirred at room temperature for 16 hours and filtered, the crystalline residue is washed with benzene and the filtrate is evaporated in vacuo. The residue is purified by means of flash chromatography on silica gel using hexane and hexane/ethyl acetate (2:1). After evaporation of the product-containing fractions and crystallization of the residue from methanol/hexane, the title compound is obtained, m.p. 96°-97° C.

후처리

  1. stirringThe reaction mixture is stirred at room temperature for 16 hours
  2. filtrationfiltered
  3. washthe crystalline residue is washed with benzene
  4. customthe filtrate is evaporated in vacuo
  5. customThe residue is purified by means of flash chromatography on silica gel
  6. customAfter evaporation of the product-containing fractions and crystallization of the residue from methanol/hexane

출처 및 근거

ORD 기록
ord-5d6b424caee3460888f1785817ac7572
출처 데이터셋
uspto-grants-1996_05
특허 번호
US05516806

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