تفاعل #5455

ord-650824152b5742c386e87f846affa28e

معادلة التفاعل

CSc1sc2c(F)c(F)c(F)cc2c(=O)c1C(=O)O
compound
CSc1sc2c(F)c(F)c(F)cc2c(=O)c1C(=O)O
3-Carboxy-2-methylthio-4-oxo-6,7,8-trifluoro-4H-1-benzothiopyran
COc1ccc(CCl)cc1
p-methoxybenzyl chloride
CCN(CC)CC
triethylamine
[I-].[Na+]
sodium iodide
COc1ccc(COC(=O)c2c(SC)sc3c(F)c(F)c(F)cc3c2=O)cc1
title compound
المردود 32.4%
COc1ccc(COC(=O)c2c(SC)sc3c(F)c(F)c(F)cc3c2=O)cc1
3-(4- Methoxybenzyloxycarbonyl)-2-methylthio-4-oxo-6,7,8-trifluoro-4H-1-benzothiopyran
المردود 32.4%

المذيبات

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    استخلاصextracted with dichloromethane
  2. 2
    غسيلThe organic layer was washed with water and with saturated saline solution
  3. 3
    تجفيفdried over anhydrous sodium sulfate
  4. 4
    تركيزconcentrated
  5. 5
    أخرىThe residue was purified by means of silica gel column chromatography (CHCl3)

الإجراء التجريبي

To a suspension of 50 mg (0.163 mmol) of the compound of Example 112 in 0.2 ml of chloroform were added 30.7 mg (0.196 mmol) of p-methoxybenzyl chloride, 16.5 mg (0.163 mmol) of triethylamine and 29.4 mg (0.196 mmol) of sodium iodide, and the mixture was stirred for 5 hours at room temperature, which was poured into ice-water and extracted with dichloromethane. The organic layer was washed with water and with saturated saline solution, dried over anhydrous sodium sulfate and concentrated. The residue was purified by means of silica gel column chromatography (CHCl3) to obtain 22.5 mg (0.0528 mmol) of title compound (yield 32%).

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US05244892uspto-grants-1993_09