تفاعل #1340628

ord-bfcd8671a708455fbc517802d58eaee3

معادلة التفاعل

COC(=O)Cc1cc(O)n(-c2ccccc2Cl)n1
methyl[1-(2-chlorophenyl)-5-hydroxy-1H-pyrazol-3-yl]acetate
COc1ccc(CC(=O)Cl)cc1
(4-methoxyphenyl)acetyl chloride
COC(=O)Cc1nn(-c2ccccc2Cl)c(O)c1C(=O)Cc1ccc(OC)cc1
methyl {1-(2-chlorophenyl)-5-hydroxy-4-[(4-methoxyphenyl)acetyl]-1H-pyrazol-3-yl}acetate
المردود 70.0%

المذيبات

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    workup.ADDITIONThe mixture of the
  2. 2
    تركيزThe resulting red solution was concentrated in vacuo
  3. 3
    أخرىto afford a red syrup that
  4. 4
    أخرىwas partitioned between ethylacetate and cold 0.1M HCl
  5. 5
    غسيلOrganic phases were washed with brine
  6. 6
    تجفيفdried over Na2SO4
  7. 7
    أخرىEvaporation of solvent

الإجراء التجريبي

The mixture of the above obtained methyl[1-(2-chlorophenyl)-5-hydroxy-1H-pyrazol-3-yl]acetate (Compound of Formula (IV), 1 g, 3.76 mmol, 1 eq.), was suspended in dioxane (10 mL) and Ca(OH)2 (0.557 g, 2 equiv.) and (4-methoxyphenyl)acetyl chloride (0.694 g) under nitrogen, was heated at 120° C. for 45-60 minutes. The resulting red solution was concentrated in vacuo to afford a red syrup that was partitioned between ethylacetate and cold 0.1M HCl. Organic phases were washed with brine and dried over Na2SO4. Evaporation of solvent gave methyl {1-(2-chlorophenyl)-5-hydroxy-4-[(4-methoxyphenyl)acetyl]-1H-pyrazol-3-yl}acetate as a pink solid (1.09 g, 70% yield, 89% HPLC purity). MS (ESI+): 415.9; MS (ESI−): 413.8.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US08455485B2uspto-grants-2013_06