تفاعل #2116

ord-ed0a8010fe1240b0b02babed64992c40

معادلة التفاعل

CCOCn1cnc2c1c(=O)n(CCCCP(=O)([O-])OCCCc1ccccc1)c(=O)n2C
benzylethyl 4-(7-ethoxymethyl-3-methylxanthin-1-yl)-butylphosphonate
N
ammonia
CCOCn1cnc2c1c(=O)n(CCCCP(=O)([O-])[O-])c(=O)n2C.CC[NH3+].CC[NH3+]
Monoethyl ammonium [4-(7-ethoxymethyl-3-methylxanthin-1-yl)butyl]-phosphonate

المذيبات

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    ترشيحThe catalyst was filtered off
  2. 2
    تركيزthe filtrate was concentrated under reduced pressure
  3. 3
    أخرىthe solution obtained
  4. 4
    أخرىafter evaporating the solvent
  5. 5
    أخرىwas then crystallized from diisopropyl ether

الإجراء التجريبي

6.3 g (0.013 mol) of benzylethyl 4-(7-ethoxymethyl-3-methylxanthin-1-yl)-butylphosphonate were hydrogenated in 100 ml of ethanol over 0.5 g of palladium (10%) on active carbon at room temperature in the course of 4 hours. The catalyst was filtered off, the filtrate was concentrated under reduced pressure, the solution obtained was treated with methanolic ammonia and the residue which remained after evaporating the solvent was then crystallized from diisopropyl ether.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US05728686uspto-grants-1998_03