تفاعل #92671

ord-648338f8760e4c67b6dc39c120fff252

الكواشف

لا شيء

المذيبات

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    أخرىequipped with a magnetic stirrer bar
  2. 2
    درجة الحرارةthe mixture heated
  3. 3
    درجة الحرارةto reflux for 40 h
  4. 4
    غسيلwashed with water (5 vol) and with brine (5 vol)
  5. 5
    غسيلeluted with methyl-tertbutyl-ether (3 vol)
  6. 6
    أخرىthe solvent was removed under reduced pressure

الإجراء التجريبي

5,6α-epoxicholestan-3β-yl butyrate (10.4 g, 22.1 mmol, 1 eq) and histamine (4.9 g, 44.1 mmol, 2 eq) were charged in a round-bottomed flask equipped with a magnetic stirrer bar. 1-Butanol (70 ml, 5 vol) was added and the mixture heated to reflux for 40 h. The reaction mixture was cooled at r.t., diluted with methyl-tertbutyl-ether (5 vol) and washed with water (5 vol) and with brine (5 vol). The organic layer was passed through a silica pad (40 g) eluted with methyl-tertbutyl-ether (3 vol) then 10% Methanol/ethyl acetate (60 vol). Fractions of interest were pooled and the solvent was removed under reduced pressure to give 5α-Hydroxy-6β-[2-(1H-imidazol-4-yl)-ethylamino]-cholestan-3β-yl butyrate as a white solid (7.8 g, 57%). In same conditions, use of ethanol as solvent (40 vol) and Ca(OTf)2 as catalyst gave a 13% yield.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US09447141B2uspto-grants-2016_09