تفاعل #51226

ord-5d8f2845c5944acb8f74eeb878fb6fd8

معادلة التفاعل

O=C(OCc1ccccc1)N1CCNCC1
N-benzyloxycarbonylpiperazine
CCCCOc1c(OCCCC)c(=O)c1=O
3,4-dibutoxy-3-cyclobutene-1,2-dione
CCCCOc1c(N2CCN(C(=O)OCc3ccccc3)CC2)c(=O)c1=O
1-benzyloxycarbonyl-4-(4-butoxy-1,2-dioxo-3-cyclobuten-3-yl)-piperazine
المردود 84.3%

الكواشف

لا شيء

المذيبات

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    تركيزThe reaction mixture was concentrated under reduced pressure
  2. 2
    أخرىthe resulting residue was purified by silica gel column chromatography (solvent: chloroform-ethyl acetate (19:1))

الإجراء التجريبي

A mixture comprising 1101 mg of N-benzyloxycarbonylpiperazine, 1131 mg of 3,4-dibutoxy-3-cyclobutene-1,2-dione and 5 ml of ethanol was stirred at room temperature for 25 hours. The reaction mixture was concentrated under reduced pressure, and the resulting residue was purified by silica gel column chromatography (solvent: chloroform-ethyl acetate (19:1)) to obtain 1570 mg of 1-benzyloxycarbonyl-4-(4-butoxy-1,2-dioxo-3-cyclobuten-3-yl)-piperazine.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US06849622B2uspto-grants-2005_02