Reaktion #531867

ord-83ab5f6921e04a558c67c436007bb3e0

Reaktionsgleichung

O
water
O=C=NC12CC3CC(CC(C3)C1)C2
1-adamantyl isocyanate
Cl.N[C@H]1CC[C@H](O)CC1
trans-4-aminocyclohexanol hydrochloride
CCN(CC)CC
triethylamine
O=C(NC12CC3CC(CC(C3)C1)C2)N[C@H]1CC[C@H](O)CC1
trans-1-(4-Hydroxy-cyclohexyl)-3-tricyclo[3.3.1.13,7]decan-1-yl-urea

Lösungsmittel

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    Sonstigethe resulting precipitates
  2. 2
    Sonstigewere collected
  3. 3
    Waschenwashed with water
  4. 4
    SonstigeThe crude product was recrystallized from methanol/water

Vorschrift

To a solution of 1-adamantyl isocyanate (10 g, 56.4 mmol) and trans-4-aminocyclohexanol hydrochloride (10.3 g, 67.7 mmol) in DMF (300 mL) was added triethylamine (6.9 g, 67.7 mmol) at 0° C. The reaction mixture was stirred overnight. The reaction mixture was poured into water, and the resulting precipitates were collected and washed with water. The crude product was recrystallized from methanol/water. Yield: 15.5 g (94% of theory). M.P.: 254° C. 1H NMR (300 MHz, DMSO-d6): δ 5.48 (d. J=9 Hz, 1H), 5.38 (s, 1H), 4.48 (d, J=4.7 Hz, 1H), 3.42-3.28 (m, 1H), 3.28-3.13 (m, 1H), 2.02-1.93 (m, 3H), 1.87-1.68 (m, 9H), 1.63-1.54 (m, 7H), 1.24-0.93 (4H).

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US08476043B2uspto-grants-2013_07