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Sodium Bicarbonate → Trifluoroacetic acid

HRID 1889142
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Reaktionsgleichung

Reaktionsgleichung von HRID 1889142
C(OC([N:8]1[CH2:12][CH2:11][C@H:10]([C@H:13]([O:16][C:17]2[CH:22]=[CH:21][C:20]([C:23]([F:26])([F:25])[F:24])=[CH:19][CH:18]=2)[CH2:14][NH2:15])[CH2:9]1)=O)(C)(C)C.[O:27]1[C:31]([C:32]2[CH:37]=[CH:36][C:35]([S:38](Cl)(=[O:40])=[O:39])=[CH:34][CH:33]=2)=[CH:30][N:29]=[CH:28]1.[C:42](=[O:45])(O)[O-:43].[Na+]>C(Cl)Cl.C(N(CC)CC)C>[O:27]1[C:31]([C:32]2[CH:33]=[CH:34][C:35]([S:38]([NH:15][CH2:14][C@H:13]([C@H:10]3[CH2:11][CH2:12][NH:8][CH2:9]3)[O:16][C:17]3[CH:18]=[CH:19][C:20]([C:23]([F:24])([F:25])[F:26])=[CH:21][CH:22]=3)(=[O:40])=[O:39])=[CH:36][CH:37]=2)=[CH:30][N:29]=[CH:28]1.[C:42]([OH:43])([C:23]([F:26])([F:25])[F:24])=[O:45]
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Komponenten

7

Edukt 3

HCID 516892Sodium BicarbonateHCID 27764154-(1,3-Oxazol-5-yl)benzenesulphonyl chlorideHCID 67776985(S)-3-[(S)-2-Amino-1-(4-trifluoromethylphenoxy)ethyl]pyrrolidine-1-carboxylic Acid t-Butyl Ester

Produkt 2

HCID 6422Trifluoroacetic acidHCID 677758584-Oxazol-5-yl-N-[(S)-2-(S)-pyrrolidin-3-yl-2-(4-trifluoromethylphenoxy)ethyl]benzenesulfonamide

Reagenzien, Katalysatoren, Lösungsmittel 2

HCID 6344DichloromethaneLösungsmittel3×HCID 8471TriethylamineLösungsmittel

Versuchsvorschrift

(S)-3-[(S)-2-Amino-1-(4-trifluoromethylphenoxy)ethyl]pyrrolidine-1-carboxylic acid t-butyl ester (35.0 mg, 0.093.5 μmol, 1.0 eq.) was dissolved in DCM (1.2 mL) and triethylamine (39.1 μL). A solution of 4-(1,3-oxazol-5-yl)benzenesulfonyl chloride (56.9 mg, 234 μmol, 2.5 eq.) in DCM (0.4 mL,) was then added. The resulting mixture was stirred for 1 hour at room temperature. Saturated sodium bicarbonate was then added (1 mL) and the mixture was diluted with DCM (2 mL). The organic layer was collected and concentrated under reduced pressure. The crude material was redissolved in 1.2 M of HCl in EtOH (1.9 mL) and stirred at room temperature overnight. The mixture was then concentrated under reduced pressure then redissolved in 1:1 AcOH/H2O (1.5 mL) and purified by preparative HPLC to yield the title compound as a TFA salt (20.1 mg). MS m/z: [M+H]+ calcd for C22H22F3N3O4S, 482.13. found 482.4.

Aufarbeitung

  1. customThe organic layer was collected
  2. concentrationconcentrated under reduced pressure
  3. dissolutionThe crude material was redissolved in 1.2 M of HCl in EtOH (1.9 mL)
  4. stirringstirred at room temperature overnight
  5. concentrationThe mixture was then concentrated under reduced pressure
  6. dissolutionthen redissolved in 1:1 AcOH/H2O (1.5 mL)
  7. custompurified by preparative HPLC

Quellen und Nachweise

ORD-Eintrag
ord-b8d32480e80446bdb227b93f8843470f
Quelldatensatz
uspto-grants-2013_08
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US08501964B2

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