Reaktion #809898

ord-58f7537ec8664bd79409308a1064b1be

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    Sonstigeprovided after workup, crude product which
  2. 2
    Sonstigetriturated with diethylether
  3. 3
    Sonstigeto give 111 mg of which
  4. 4
    Sonstigewas further purified by recrystallization from ethylacetate/hexanes

Vorschrift

Reaction of α-phenylcyclopentaneacetyl chloride (Prepared in Example 12, Step1) and 2-Amino-3-cyano-5,6-dihydro-4H-cyclopenta[b]thiophene (164 mg; 1.0 mmol) according to the procedure outlined in Example 5 for 20 h at room temperature provided after workup, crude product which triturated with diethylether to give 111 mg of which was further purified by recrystallization from ethylacetate/hexanes to provide 44 mg (%) of N-(3-Cyano-5,6-dihydro-4H-cyclopenta[b]thiophen-2-yl)-2-cyclopentyl-2-phenyl-acetamide as a light brown solid. EI-HRMS m/e calcd for C21H32N2OS (M+) 350.1453, found 350.1456.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US07138529B2uspto-grants-2006_11