تفاعل #2200603

ord-364ad44143e745ab9de8bf01d6c7f61c

معادلة التفاعل

Clc1ncnc2[nH]ccc12
6-Chloro-7-deazapurine
O=C1CCC(=O)N1I
N-iodosuccinimide
Clc1ncnc2[nH]cc(I)c12
title compound
المردود 83.0%
Clc1ncnc2[nH]cc(I)c12
6-Chloro-7-iodo-7-deazapurine
المردود 83.0%

الكواشف

لا شيء

المذيبات

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    workup.WAITleft at ambient temperature in the darkness over night
  2. 2
    أخرىThe solvent was evaporated
  3. 3
    غسيلOrganic fraction was washed with 10% Na2SO3 (2×100 ml), brine (150 ml)
  4. 4
    تجفيفdried over Na2SO4
  5. 5
    أخرىevaporated
  6. 6
    أخرىThe yellow residue was crystallized from ethanol

الإجراء التجريبي

6-Chloro-7-deazapurine 10.75 g (70 mmol) and N-iodosuccinimide (16.8 g, 75 mmol) were dissolved in 400 ml of dry DMF and left at ambient temperature in the darkness over night. The solvent was evaporated. The dark residue was distributed between 500 ml of ethyl acetate and 150 ml of 10% Na2SO3. Organic fraction was washed with 10% Na2SO3 (2×100 ml), brine (150 ml), dried over Na2SO4 and evaporated. The yellow residue was crystallized from ethanol to yield 16.2 g (83%) of the title compound as off white crystals. The mother liquid was evaporated, dissolved in toluene, and purified by flush chromatography on silica gel (7×4 cm). The column was washed with toluene until the eluent was colorless than the title compound was eluted with 5% ethyl acetate in toluene to give additional 3.5 g of the title product.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US07432248B2uspto-grants-2008_10