Réaction #531872

ord-9bb1f97f3091440392d95bed10ae1ca6

Équation de réaction

O
water
CCN(CC)CC
triethylamine
N[C@H]1CC[C@@H](Oc2ccc(F)cc2)CC1
compound 10
N[C@H]1CC[C@@H](Oc2ccc(F)cc2)CC1
cis-4-(4-Fluoro-phenoxy)-cyclohexylamine
O=C=NC12CC3CC(CC(C3)C1)C2
1-adamantyl isocyanate
O=C(NC12CC3CC(CC(C3)C1)C2)N[C@H]1CC[C@@H](Oc2ccc(F)cc2)CC1
cis-1-[4-(4-Fluoro-phenoxy)-cyclohexyl]-3-tricyclo[3.3.1.13,7]decan-1-yl-urea

Solvants

Conditions de réaction

Conditions détaillées
See reaction.notes.procedure_details.

Traitement

  1. 1
    Autrethe resulting precipitates
  2. 2
    Autrewere collected
  3. 3
    Lavagewashed with water
  4. 4
    AutreThe crude product was recrystallized from DCM/hexanes

Mode opératoire

To a solution compound 10 in DMF was added 1-adamantyl isocyanate (0.16 g, 0.91 mmol) followed by triethylamine (0.10 g, 1.0 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 DCM/hexanes. Yield: 0.31 g (88% of theory). M.P.: 207° C. 1H NMR (300 MHz, CDCl3): δ 6.98-6.91 (m, 2H), 6.84-6.78 (m, 2H), 4.34 (s, 1H), 4.30 (d, J=9.8 Hz, 1H), 4.20 (s, 1H), 3.71-3.56 (m, 1H), 2.13-1.44 (m, 23H).

Source

DOI: 10.6084/m9.figshare.5104873.v1Brevet: US08476043B2uspto-grants-2013_07