Hydrochloric Acid → N1-(5-p-methylphenyloxazol-2-yl)-5,6,7,8-tetrahydronaphthalene-1,7-diamine

HRID 600809

Reaktionsgleichung

Reaktionsgleichung von HRID 600809
Cl.C(OC(=O)[NH:8][CH:9]1[CH2:18][CH2:17][C:16]2[C:11](=[C:12]([NH:19][C:20]3[O:21][C:22]([C:25]4[CH:30]=[CH:29][C:28]([CH3:31])=[CH:27][CH:26]=4)=[CH:23][N:24]=3)[CH:13]=[CH:14][CH:15]=2)[CH2:10]1)(C)(C)C>O1CCOCC1>[CH3:31][C:28]1[CH:29]=[CH:30][C:25]([C:22]2[O:21][C:20]([NH:19][C:12]3[C:11]4[CH2:10][CH:9]([NH2:8])[CH2:18][CH2:17][C:16]=4[CH:15]=[CH:14][CH:13]=3)=[N:24][CH:23]=2)=[CH:26][CH:27]=1

Komponenten

4

Versuchsvorschrift

Hydrogen chloride in dioxane (4N, 7 mL, 28 mmol) was added to a suspension of 199 mg (0.474 mmol) of the product of Example 20G in 1 mL dioxane. After stirring 45 minutes, the mixture was quenched with 3N NaOH solution, then diluted with EtOAc and poured into water. The separated organic phase was washed with brine, dried (Na2SO4), filtered and concentrated under reduced pressure. The crude product was triturated with Et2O and the solid was collected by vacuum filtration. The result was 92 mg (61%) of the title compound as a pale pink solid. 1H NMR (DMSO-d6) δ 9.02 (br s, 1H), 7.57 (d, J=7.1 Hz, 1H), 7.45 (d, J=8.1 Hz, 2H), 7.28 (s, 1H), 7.23 (d, J=8.1 Hz, 2H), 7.08 (t, J=7.8 Hz, 1H), 6.83 (d, J=7.1 Hz, 1H), 3.05-2.70 (m, 4H), 2.31 (m, 4H), 1.85 (m, 3H), 1.42 (m, 1H); MS (ESI+) m/z 320 (M+H)+.

Aufarbeitung

  1. customthe mixture was quenched with 3N NaOH solution
  2. additiondiluted with EtOAc
  3. additionpoured into water
  4. washThe separated organic phase was washed with brine
  5. dry with materialdried (Na2SO4)
  6. filtrationfiltered
  7. concentrationconcentrated under reduced pressure
  8. customThe crude product was triturated with Et2O
  9. filtrationthe solid was collected by vacuum filtration

Quellen und Nachweise

ORD-Eintrag
ord-c6b6c8bde45c42ea907b482b8340cf78
Quelldatensatz
uspto-grants-2011_03
Patentnummer
US07902236B2

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