Hydrochloric Acid → Ammonium Hydroxide

HRID 1367235Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 1367235
Cl.C([S@@]([NH:8][C@H:9]([C:31]1[CH:36]=[C:35]([F:37])[CH:34]=[C:33]([F:38])[CH:32]=1)[CH2:10][CH2:11][C@@:12]1([C:27]([O:29]C)=O)[CH2:16][CH2:15][CH2:14][N:13]1[C:17]([O:19][CH2:20][C:21]1[CH:26]=[CH:25][CH:24]=[CH:23][CH:22]=1)=[O:18])=[O:7])(C)(C)C.C(N(CC)CC)C>CO>[NH4+:8].[OH-:7].[F:38][C:33]1[CH:32]=[C:31]([C@@H:9]2[CH2:10][CH2:11][C@@:12]3([N:13]([C:17]([O:19][CH2:20][C:21]4[CH:22]=[CH:23][CH:24]=[CH:25][CH:26]=4)=[O:18])[CH2:14][CH2:15][CH2:16]3)[C:27](=[O:29])[NH:8]2)[CH:36]=[C:35]([F:37])[CH:34]=1

Komponenten

6

Versuchsvorschrift

HCl (g) was bubbled through a solution of 1-benzyl 2-methyl (2R)-2-[(3S)-3-{[(S)-tert-butylsulfinyl]amino}-3-(3,5-difluorophenyl)propyl]pyrrolidine-1,2-dicarboxylate from Step C (1.02 g, 1.90 mmol) in MeOH (25 mL) at 0° C. for 1 min. After stirring for 1 h, the reaction mixture was concentrated to dryness in vacuo. To the crude product suspended in toluene (25 mL) was added triethylamine (2.12 mL, 15.2 mmol), and the reaction mixture was heated to reflux for 66 h. The reaction mixture was concentrated in vacuo and the crude product was purified by silica gel chromatography, eluting with a gradient of CH2Cl2:MeOH:NH4OH—100:0:0 to 95:5:1, to give the title compound. MS: m/z=401 (M+1).

Aufarbeitung

  1. concentrationthe reaction mixture was concentrated to dryness in vacuo
  2. temperaturethe reaction mixture was heated
  3. temperatureto reflux for 66 h
  4. concentrationThe reaction mixture was concentrated in vacuo
  5. customthe crude product was purified by silica gel chromatography
  6. washeluting with a gradient of CH2Cl2

Quellen und Nachweise

ORD-Eintrag
ord-f423c372f145486ba62a7e92895fdb76
Quelldatensatz
uspto-grants-2011_02
Patentnummer
US07893079B2

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