تفاعل #690409

ord-a7a8c628b3734f0b83263f9f2503b693

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    أخرىexcept that after purification of the residue on a Redisep® silica column
  2. 2
    غسيلeluting with ethyl acetate/MeOH (30:70)
  3. 3
    أخرىthe solid, after precipitation from CH2Cl2 with isohexane
  4. 4
    أخرىwas further purified on an SCX column
  5. 5
    غسيلeluting sequentially with ethyl acetate, MeOH and 1% ammonia/MeOH

الإجراء التجريبي

Benzyl 2-[(4-{[(3,4-dichlorophenyl)amino]carbonyl}piperazin-1-yl)methyl]piperazine-1-carboxylate and acetaldehyde were used in a similar manner to N-(3,4-dichlorophenyl)-4-{[(2S)-4-(2-pyridin-3-ylethyl)morpholin-2-yl]methyl}piperazine-1-carboxamide, except that after purification of the residue on a Redisep® silica column, eluting with ethyl acetate/MeOH (30:70), the solid, after precipitation from CH2Cl2 with isohexane, was further purified on an SCX column, eluting sequentially with ethyl acetate, MeOH and 1% ammonia/MeOH to give the title product (20 mg, 18%).

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US07906645B2uspto-grants-2011_03