Hydrochloric Acid → (S)-3-[1-(2,3,6-Trichlorophenoxy)prop-2-ynyl]pyrrolidine

HRID 588016

Reaktionsgleichung

Reaktionsgleichung von HRID 588016
C(OC([N:8]1[CH2:12][CH2:11][C@H:10]([CH:13]([OH:16])[C:14]#[CH:15])[CH2:9]1)=O)(C)(C)C.CC(OC(/N=N/C(OC(C)C)=O)=O)C.C1(C)C=CC=CC=1.C1C=CC(P(C2C=CC=CC=2)C2C=CC=CC=2)=CC=1.[Cl:57][C:58]1[C:63]([Cl:64])=[CH:62][CH:61]=[C:60]([Cl:65])[C:59]=1O.C1(O)C=CC=CC=1.Cl.CCO>>[Cl:57][C:58]1[C:63]([Cl:64])=[CH:62][CH:61]=[C:60]([Cl:65])[C:59]=1[O:16][CH:13]([C@H:10]1[CH2:11][CH2:12][NH:8][CH2:9]1)[C:14]#[CH:15]

Komponenten

9

Reaktionsbedingungen

Temperatur
100 °C

Versuchsvorschrift

A mixture of (S)-3-(1-hydroxyprop-2-ynyl)pyrrolidine-1-carboxylic acid t-butyl ester (21.0 mg, 93.2 μmol) and DIAD (22.0 μL, 112 μmol) was dissolved in toluene (65 μL, 610 μmol) at room temperature. PPh3 (29.3 mg, 112 μmol) and 2,3,6-trichlorophenol (20.2 mg, 102 μmol) were dissolved in toluene (0.1 mL, 1 mmol) and heated at 100° C. The t-butyl ester mixture was slowly added into the phenol mixture at 100° C., and stirred for 1 hour. The mixture was then removed from the heat and stirred at room temperature overnight. The mixture was then concentrated and the resulting residue was treated with 1.25M HCl in EtOH (0.6 mL, 0.8 mmol) at room temperature overnight. The mixture was concentrated and the residue was redissolved in a mixture of 50% AcOH/H2O (1.4 mL) and McCN (0.2 mL), filtered and purified by reverse phase preparative HPLC to yield the title compound as a mono-TFA salt (21.2 mg, 99% purity). MS in/z: [M+H]+ calcd for C13H12Cl3NO, 304.00. found 304.0.

Aufarbeitung

  1. customThe mixture was then removed from the
  2. temperatureheat
  3. stirringstirred at room temperature overnight
  4. concentrationThe mixture was then concentrated
  5. concentrationThe mixture was concentrated
  6. dissolutionthe residue was redissolved in a mixture of 50% AcOH/H2O (1.4 mL) and McCN (0.2 mL)
  7. filtrationfiltered
  8. custompurified by reverse phase preparative HPLC

Quellen und Nachweise

ORD-Eintrag
ord-bd778949c447438a8b71187d81362d7f
Quelldatensatz
uspto-grants-2016_01
Patentnummer
US09227933B2

Verknüpfte Notizen

Wird geladen…