Trifluoroacetic acid → (S)-3-[5-(1-amino-2-biphenyl-4-yl-ethyl)-tetrazol-1-yl]-propionitrile trifiuoroacetate salt

HRID 1078673Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 1078673
C(OC([NH:8][C@H:9]([C:23]1[N:27]([CH2:28][CH2:29][C:30]#[N:31])[N:26]=[N:25][N:24]=1)[CH2:10][C:11]1[CH:16]=[CH:15][C:14]([C:17]2[CH:22]=[CH:21][CH:20]=[CH:19][CH:18]=2)=[CH:13][CH:12]=1)=O)(C)(C)C.[F:32][C:33]([F:38])([F:37])[C:34]([OH:36])=[O:35]>C(Cl)Cl>[F:32][C:33]([F:38])([F:37])[C:34]([OH:36])=[O:35].[NH2:8][C@H:9]([C:23]1[N:27]([CH2:28][CH2:29][C:30]#[N:31])[N:26]=[N:25][N:24]=1)[CH2:10][C:11]1[CH:16]=[CH:15][C:14]([C:17]2[CH:22]=[CH:21][CH:20]=[CH:19][CH:18]=2)=[CH:13][CH:12]=1

Komponenten

4

Versuchsvorschrift

(S)-3-[5-(1-t-butoxycarbonylamino-2-biphenyl-4-yl-ethyl)-tetrazol-1-yl]-propionitrile (9.22 g, 22 mmol) is dissolved in methylene chloride (135 mL) under nitrogen. To the stirred solution is added trifiuoroacetic acid (50 mL). After 50 minutes, the solution is concentrated under reduced pressure and the residue is treated with ether (200 mL). The amorphous solid is filtered off, washed with ether and dried under vacuum at 45° for 2 hours, then at room temperature for 18 hours to yield (S)-3-[5-(1-amino-2-biphenyl-4-yl-ethyl)-tetrazol-1-yl]-propionitrile trifiuoroacetate salt, m.p. 211°-212°, [α]D =+23.35° (c 1.05, DMSO).

Aufarbeitung

  1. concentrationthe solution is concentrated under reduced pressure
  2. additionthe residue is treated with ether (200 mL)
  3. filtrationThe amorphous solid is filtered off
  4. washwashed with ether
  5. customdried under vacuum at 45° for 2 hours

Quellen und Nachweise

ORD-Eintrag
ord-604265b5acb849948e4c7de61d518f33
Quelldatensatz
uspto-grants-1996_08
Patentnummer
US05550119

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