تفاعل #1121784

ord-f79edbf0b51b4ab298bee8749f1db8a2

معادلة التفاعل

O
water
c1ccc(COc2ncnc3nc[nH]c23)cc1
6-Benzyloxypurine
O=C([O-])[O-].[K+].[K+]
potasiumcarbonate
COC(=O)CBr
bromoacetic acid methyl ester
COC(=O)Cn1cnc2c(OCc3ccccc3)ncnc21
Methyl(6-(Benzyloxy)purin-9-yl)acetate

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    تجفيفThe organic phase was dried over magnesium sulphate
  2. 2
    أخرىevaporated to a volume of ˜10 ml
  3. 3
    أخرىprecipitated with pet. ether
  4. 4
    أخرىThe two products were separated by column chromatography
  5. 5
    أخرىThe products was precipitated in pet. ether

الإجراء التجريبي

6-Benzyloxypurine (4.18 g; 18.5 mmol) was added to a suspension of potasiumcarbonate (3.1 g; 22.4 mmol) in DMF (100 ml). After 15 min. bromoacetic acid methyl ester (1.93 ml; 20.4 mmol) was added. The reaction was monitored by TLC in butanol:acetic acid:water 4:1:1. Upon completion, the reaction mixture was portioned between water (600 ml) and ethylacetate (600 ml). The organic phase was dried over magnesium sulphate and evaporated to a volume of ˜10 ml and precipitated with pet. ether. The two products were separated by column chromatography using ethylacetate as the solvent. The products was precipitated in pet. ether. Yield: 2.36 g (43%). Melting point: 111.5-115° C. UV λmax=250 nm (9-alkylated); λmax=260 nm (7-alkylated). 1H-NMR (DMSO-d6): 8.60 (1H, s); 8.43 (1H, s); 7.6-7.35 (5H, m); 5.69 (2H, s); 5.26 (2H, s); 3.75 (3H, s).

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US08546309B2uspto-grants-2013_10