تفاعل #4486

ord-7107d45708c94d15882a5699664f3c58

معادلة التفاعل

O=C1CCC(=O)N1Br
N-Bromosuccinimide
Cc1oc(-c2ccccc2)nc1CCOc1ccc(CC2SC(=O)NC2=O)cc1
5-{4-[2-(5-methyl-2-phenyl-4-oxazolyl)ethoxy]benzyl}-2,4-thiazolidinedione
CC(C)(C#N)N=NC(C)(C)C#N
α,α'-azobisisobutyronitrile
O=C1NC(=O)C(Cc2ccc(OCCc3nc(-c4ccccc4)oc3CBr)cc2)S1
5-{4-[2-(5-bromomethyl-2-phenyl-4-oxazolyl)ethoxy]benzyl}-2,4-thiazolidinedione

المذيبات

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    درجة الحرارةunder reflux
  2. 2
    درجة الحرارةAfter refluxing for another 10 minutes
  3. 3
    غسيلthe reaction mixture was washed with water
  4. 4
    تجفيفdried (MgSO4)
  5. 5
    workup.DISTILLATIONThe solvent was distilled off

الإجراء التجريبي

N-Bromosuccinimide (2.75 g) was added portionwise to a solution of 5-{4-[2-(5-methyl-2-phenyl-4-oxazolyl)ethoxy]benzyl}-2,4-thiazolidinedione (6.0 g) and α,α'-azobisisobutyronitrile (0.5 g) in carbon tetrachloride(150 ml) under reflux. After refluxing for another 10 minutes, the reaction mixture was washed with water and dried (MgSO4). The solvent was distilled off to give 5-{4-[2-(5-bromomethyl-2-phenyl-4-oxazolyl)ethoxy]benzyl}-2,4-thiazolidinedione as a crude oily substance (about 8 g). IR (neat) cm-1 : 1750, 1690. NMRδ(ppm) in CDCl3 : 3.03 (2 HtJ=7 Hz), 2.9 to 3.2 (1H, m), 3.48 (1H, d.d, J=14 and 5 Hz), 4.24 (2H, t, J=7 Hz), 4.45 (1h, d.d, J=9 and 5 Hz), 4.61 (2H, s), 6.81 (2H, d, J=9 Hz), 7.10 (2H, d, J=9 Hz), 7.4 (3H, m), 8.0 (2H, m), 8.70 (1H, broad s).

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US04725610uspto-grants-1988_02