Sodium Chloride → HCID 13366924, 화합물

HRID 1632937노트

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HRID 1632937 반응식
[CH2:1]([O:8][C:9]([NH:11][CH:12]1[CH2:15][NH:14][C:13]1=[O:16])=[O:10])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.C([Li])(CC)C.Cl[C:23]1[CH:28]=[CH:27][CH:26]=[CH:25][C:24]=1[P:29](=O)([O-:33])[O:30][CH2:31][CH3:32].[Cl-].[Na+]>O1CCCC1>[CH2:31]([O:30][P:29]([C:24]1[CH:25]=[CH:26][CH:27]=[CH:28][CH:23]=1)([N:14]1[CH2:15][C@H:12]([NH:11][C:9](=[O:10])[O:8][CH2:1][C:2]2[CH:3]=[CH:4][CH:5]=[CH:6][CH:7]=2)[C:13]1=[O:16])=[O:33])[CH3:32]

참가 물질

6

실험 절차

To a solution of 3-benzyloxycarbonylamino-2-azetidinone (5.0 g) in dry tetrahydrofuran (125 ml), cooled to -78° C., was added sec-butyl lithium (18.5 ml) and the mixture was stirred for 5 minutes. Ethyl chlorophenylphosphonate (4.71 g) was added and the mixture was stirred for 1 hour at -78° C. followed by the addition of 125 ml of saturated sodium chloride solution. The mixture was then extracted twice with 125 ml portions of ethyl acetate and the extracts were combined, dried over anhydrous sodium sulfate and the solvent removed in vacuo yielding the crude product as a foam. The crude product was purified by chromatography on silica gel (750 g), eluting with dichloromethane:ethyl acetate (1:1) followed by ethyl acetate. The ethyl acetate fractions were stripped and the residue triturated with ether to yield 4.94 g of product.

후처리

  1. stirringthe mixture was stirred for 1 hour at -78° C.
  2. extractionThe mixture was then extracted twice with 125 ml portions of ethyl acetate
  3. dry with materialdried over anhydrous sodium sulfate
  4. customthe solvent removed in vacuo
  5. customyielding the crude product as a foam
  6. customThe crude product was purified by chromatography on silica gel (750 g)
  7. washeluting with dichloromethane:ethyl acetate (1:1)
  8. customthe residue triturated with ether

출처 및 근거

ORD 기록
ord-87b604cc0b97427c814f2ae5240a2609
출처 데이터셋
uspto-grants-1984_10
특허 번호
US04478749

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