Hydrochloric Acid → 1-[(3-Oxo-2-oxa-bicyclo[2.2.1]heptane-5-carbonyl)-amino]-2-vinyl-cyclo-propane carboxylic acid ethyl ester

HRID 643849ノート

反応式

HRID 643849 の反応式
[O:1]=[C:2]1[CH:7]2[CH2:8][CH:4]([CH2:5][CH:6]2[C:9]([OH:11])=O)[O:3]1.Cl.[CH2:13]([O:15][C:16]([C:18]1([NH2:23])[CH2:20][CH:19]1[CH:21]=[CH2:22])=[O:17])[CH3:14].CN(C(ON1N=NC2C=CC=NC1=2)=[N+](C)C)C.F[P-](F)(F)(F)(F)F.CCN(C(C)C)C(C)C>CN(C=O)C.C(Cl)Cl>[CH2:13]([O:15][C:16]([C:18]1([NH:23][C:9]([CH:6]2[CH2:5][CH:4]3[CH2:8][CH:7]2[C:2](=[O:1])[O:3]3)=[O:11])[CH2:20][CH:19]1[CH:21]=[CH2:22])=[O:17])[CH3:14]

参加物

8

実験手順

To a solution of 33 (857 mg, 5.5 mmol), in DMF (14 mL) and DCM (25 mL) at room temperature, was added the hydrochloride of 1-amino-2-vinyl-cyclopropanecarboxylic acid ethyl ester, prepared as described in WO03/099274, (1.15 g, 6.0 mmol), HATU (2.29 g, 6.0 mmol) and DIPEA (3.82 mL, 22 mmol). The reaction was stirred under N2-atmosphere at ambient temperature for 1 h. LC/MS analysis showed complete conversion and the reaction mixture was concentrated in vacuo. The residue was redissolved in DCM (100 mL) and 0.1 M HCl (aq) and the phases were separated. The organic phase was washed with NaHCO3 (aq) and brine, dried (MgSO4) and filtered. Removal of the solvent in vacuo afforded the target compound (1.6 g, 99%). LC/MS>95%, m/z (ESI+)=294 (MH+)

後処理

  1. customprepared
  2. concentrationthe reaction mixture was concentrated in vacuo
  3. dissolutionThe residue was redissolved in DCM (100 mL)
  4. custom0.1 M HCl (aq) and the phases were separated
  5. washThe organic phase was washed with NaHCO3 (aq) and brine
  6. dry with materialdried (MgSO4)
  7. filtrationfiltered
  8. customRemoval of the solvent in vacuo

出典と根拠

ORDレコード
ord-1b7eff7ec619485a9872c5737bd8e6e1
出典データセット
uspto-grants-2010_04
特許番号
US07700552B2

反応ノート

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