Dicyclohexylcarbodiimide → (R)-quinuclidin-3-yl 2-(3-fluorophenyl)-2-(phenylamino)acetate

HRID 1044044Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 1044044
C1CCC(N=C=NC2CCCCC2)CC1.Cl.[F:17][C:18]1[CH:19]=[C:20]([CH:24]([NH:28][C:29]2[CH:34]=[CH:33][CH:32]=[CH:31][CH:30]=2)[C:25]([OH:27])=[O:26])[CH:21]=[CH:22][CH:23]=1.C1C=CC2N(O)N=NC=2C=1.[N:45]12[CH2:52][CH2:51][CH:48]([CH2:49][CH2:50]1)[C@@H:47](O)[CH2:46]2>C1COCC1>[F:17][C:18]1[CH:19]=[C:20]([CH:24]([NH:28][C:29]2[CH:34]=[CH:33][CH:32]=[CH:31][CH:30]=2)[C:25]([O:27][C@@H:47]2[CH:48]3[CH2:51][CH2:52][N:45]([CH2:50][CH2:49]3)[CH2:46]2)=[O:26])[CH:21]=[CH:22][CH:23]=1

Komponenten

6

Versuchsvorschrift

PS-DCC (982 mg, 1.31 mmol, loading: 1.33 mmol/g) was suspended in dry THF (15 ml). 2-(3-Fluorophenyl)-2-(phenylamino)acetic acid hydrochloride (I17) (184 mg, 0.65 mmol), HOBT (200 mg, 1.31 mmol), and (R)-quinuclidin-3-ol (249 mg, 1.96 mmol) were added, and the mixture was shaken at room temperature overnight. PS-DCC was removed by filtration, and the filtrate is evaporated. The residue was dissolved in EtOAc and washed with NaHCO3, water and brine. The organic layer was dried over Na2SO4, filtered, and evaporated to dryness. The crude compound was purified by filtration through a pad of silica-gel using DCM/MeOH=9/1 as the eluent. The title compound was obtained (129 mg, 56% yield, mixture of diastereomers).

Aufarbeitung

  1. customPS-DCC was removed by filtration
  2. customthe filtrate is evaporated
  3. dissolutionThe residue was dissolved in EtOAc
  4. washwashed with NaHCO3, water and brine
  5. dry with materialThe organic layer was dried over Na2SO4
  6. filtrationfiltered
  7. customevaporated to dryness
  8. filtrationThe crude compound was purified by filtration through a pad of silica-gel

Quellen und Nachweise

ORD-Eintrag
ord-143b2466e3c645319cfab185e67cf7e2
Quelldatensatz
uspto-grants-2013_10
Patentnummer
US08563577B2

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