تفاعل #51519

ord-75b6f31520a04d588ebf5478b3981902

معادلة التفاعل

C=CCBr
allyl bromide
Nc1ncnc2c1ncn2[C@@H]1O[C@H](CO)[C@@H](O)[C@H]1O
Adenosine
O=P12OP3(=O)OP(=O)(O1)OP(=O)(O2)O3
P2O5
[H-].[Na+]
Sodium hydride
C=CCO[C@H]1[C@@H](O)[C@H](n2cnc3c(N)ncnc32)O[C@@H]1CO
title compound
المردود 66.0%
C=CCO[C@H]1[C@@H](O)[C@H](n2cnc3c(N)ncnc32)O[C@@H]1CO
3′-O-allyl adenosine
المردود 66.0%

الكواشف

لا شيء

المذيبات

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    أخرىDMF was removed under vacuum and residue
  2. 2
    غسيلwas washed with ethyl acetate (100 mL)
  3. 3
    أخرىEthyl acetate layer was decanted
  4. 4
    أخرىFiltrate obtained
  5. 5
    غسيلeluted with 10% MeOH in CH2Cl2

الإجراء التجريبي

Adenosine (20 g, 74.84 mmol) was dried over P2O5 under high vacuum at 40° C. for two days. It was then suspended in DMF under inert atmosphere. Sodium hydride (2.5 g, 74.84 mmol, 60% dispersion in mineral oil), stirred at room temperature for 10 minutes. Then allyl bromide (7.14 mL, 82.45 mmol) was added dropwise and the reaction mixture was stirred at room temperature overnight. DMF was removed under vacuum and residue was washed with ethyl acetate (100 mL). Ethyl acetate layer was decanted. Filtrate obtained contained product. It was then placed on a flash column and eluted with 10% MeOH in CH2Cl2 to get the title compound (15.19 g, 66%). Rf 0.4, 0.4a ((10% MeOH in CH2Cl2)

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US06849723B2uspto-grants-2005_02