تفاعل #336944

ord-95f15adcd3274c0687acf6b809a83c71

معادلة التفاعل

O=c1[nH]c(=O)c2c(ncn2Cc2ccccc2)[nH]1
7-Benzyl-3,7-dihydro-1H-purine-2,6-dione
O=C([O-])[O-].[Na+].[Na+]
sodium carbonate
CCCCCI
1-iodopentane
CCCCCn1c(=O)[nH]c(=O)c2c1ncn2Cc1ccccc1
desired product
المردود 44.0%
CCCCCn1c(=O)[nH]c(=O)c2c1ncn2Cc1ccccc1
7-Benzyl-3-pentyl-3,7-dihydro-1H-purine-2,6-dione
المردود 44.0%

المذيبات

ظروف التفاعل

درجة الحرارة
40°CELSIUS
الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    استخلاصThe aqueous layer was extracted with EtOAc twice
  2. 2
    أخرىThe combined organic layers were dried
  3. 3
    ترشيحfiltered
  4. 4
    تركيزconcentrated
  5. 5
    أخرىThe resulting white solid was collected
  6. 6
    أخرىdried in vacuum oven at 50° C. for 18 h

الإجراء التجريبي

7-Benzyl-3,7-dihydro-1H-purine-2,6-dione (5.0 g, 21 mmol) was mixed with sodium carbonate (3.3 g, 31 mmol) and 1-iodopentane (4.0 mL, 31 mmol) in DMF (60 mL). After being stirred at 40° C. for 18 h, the reaction mixture was diluted with water and EtOAc. The aqueous layer was extracted with EtOAc twice. The combined organic layers were dried, filtered and concentrated. The resulting white solid was collected and dried in vacuum oven at 50° C. for 18 h to provide the desired product (2.84 g, 44% yield). LCMS calculated for C17H21N4O2(M+H): 313.2. found: 313.2.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US07863285B2uspto-grants-2011_01