Methyl iodide → 5-(S)-Azidomethyl-3-[4'-methylthio-3'-fluorophenyl]oxazolidine-2-one

HRID 351883ノート

反応式

HRID 351883 の反応式
C(O)(C(F)(F)F)=O.C([SiH](C(C)C)C(C)C)(C)C.[N:18]([CH2:21][C@H:22]1[O:26][C:25](=[O:27])[N:24]([C:28]2[CH:33]=[CH:32][C:31]([S:34][C:35](C3C=CC=CC=3)(C3C=CC=CC=3)C3C=CC=CC=3)=[C:30]([F:54])[CH:29]=2)[CH2:23]1)=[N+:19]=[N-:20].IC.C(N(CC)CC)C>C(Cl)Cl>[N:18]([CH2:21][C@H:22]1[O:26][C:25](=[O:27])[N:24]([C:28]2[CH:33]=[CH:32][C:31]([S:34][CH3:35])=[C:30]([F:54])[CH:29]=2)[CH2:23]1)=[N+:19]=[N-:20]

参加物

7

反応物 5

HCID 6328Methyl iodideHCID 6422Trifluoroacetic acidHCID 8471TriethylamineHCID 138754Silane, tris(1-methylethyl)-HCID 229662215-(S)-azidomethyl-3-[4'-triphenylmethylthio-3'-fluorophenyl]-oxazolidine-2-one

生成物 1

HCID 229662145-(S)-Azidomethyl-3-[4'-methylthio-3'-fluorophenyl]oxazolidine-2-one収率 90%

試薬・触媒・溶媒 1

HCID 6344Dichloromethane溶媒

実験手順

5% TFA and 2.5% triisopropylsilane in DCM (4 ml) was added to 5-(S)-azidomethyl-3-[4′-triphenylmethylthio-3′-fluorophenyl]oxazolidine-2-one (0.250 g, 0.490 mmol; prepared as described above for Example 6), and the mixture stirred for 1 h at r.t. Solvent was removed under vacuum and the residue dissolved in DMF (2 ml). Iodomethane (0.046 ml, 0.735 mmol) was added followed by dropwise addition of triethylamine (0.136 ml, 0.979 mmol). The mixture was stirred at r.t. for 2 h, evaporated, and the residue purified by PTLC (50% ethyl acetate in DCM) to give the product as a white solid (0.124 g, 90%). MS (m/z): [M+H]+=283.

後処理

  1. customSolvent was removed under vacuum
  2. dissolutionthe residue dissolved in DMF (2 ml)
  3. stirringThe mixture was stirred at r.t. for 2 h
  4. customevaporated
  5. customthe residue purified by PTLC (50% ethyl acetate in DCM)

出典と根拠

ORDレコード
ord-33402d1c398247ebb8f744b85390b18d
出典データセット
uspto-grants-2004_06
特許番号
US06743811B2

反応ノート

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