تفاعل #2286282

ord-5f22e7a4100847a0b6eb6f2dd78f20b0

معادلة التفاعل

COC(=O)Cc1cc(C)c(Oc2cc(C(C)C)c(Cl)nn2)c(C)c1
[4-(6-chloro-5-isopropyl-pyridazin-3-yloxy)-3,5-dimethyl-phenyl]-acetic acid methyl ester
COC(=O)Cc1cc(C)c(Oc2cc(C(C)C)c(Cl)nn2)c(C)c1
[4-(6-Chloro-5-isopropyl-pyridazin-3-yloxy)-3,5-dimethyl-phenyl]-acetic acid methyl ester
[Na+].[OH-]
sodium hydroxide
Cc1cc(CC(=O)O)cc(C)c1Oc1cc(C(C)C)c(Cl)nn1
[4-(6-chloro-5-isopropyl-pyridazin-3-yloxy)-3,5-dimethyl-phenyl]-acetic acid
Cc1cc(CC(=O)O)cc(C)c1Oc1cc(C(C)C)c(Cl)nn1
[4-(6-Chloro-5-isopropyl-pyridazin-3-yloxy)-3,5-dimethyl-phenyl]-acetic acid

المذيبات

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    أخرىat room temperature
  2. 2
    تركيزAt this time, the reaction mixture was concentrated under vacuum
  3. 3
    workup.ADDITIONThe resulting solid was diluted with water (200 mL)
  4. 4
    استخلاصextracted with ethyl acetate (200 mL)
  5. 5
    workup.ADDITIONThe water layer was acidified to pH=4 by the addition of a 1N aqueous hydrochloric acid solution
  6. 6
    استخلاصwas extracted with ethyl acetate (2×200 mL)
  7. 7
    غسيلwashed with a saturated aqueous sodium chloride solution
  8. 8
    تجفيفdried with magnesium sulfate
  9. 9
    ترشيحfiltered
  10. 10
    تركيزconcentrated under vacuum
  11. 11
    أخرىto afford a solid
  12. 12
    أخرىThe solid was dried overnight under high vacuum

الإجراء التجريبي

A solution of [4-(6-chloro-5-isopropyl-pyridazin-3-yloxy)-3,5-dimethyl-phenyl]-acetic acid methyl ester (8a) (1.66 g, 4.75 mmol, contains a minor amount of isomer) in methanol (50 mL) at room temperature was treated dropwise with a 1N aqueous sodium hydroxide solution (9.5 mL, 9.50 mmol). The reaction was stirred at room temperature for 24 h. At this time, the reaction mixture was concentrated under vacuum. The resulting solid was diluted with water (200 mL) and extracted with ethyl acetate (200 mL). The ethyl acetate layer was discarded. The water layer was acidified to pH=4 by the addition of a 1N aqueous hydrochloric acid solution and was extracted with ethyl acetate (2×200 mL). The organic layers were combined, washed with a saturated aqueous sodium chloride solution, dried with magnesium sulfate, filtered and concentrated under vacuum to afford a solid. The solid was dried overnight under high vacuum to afford [4-(6-chloro-5-isopropyl-pyridazin-3-yloxy)-3,5-dimethyl-phenyl]-acetic acid (9a) (1.58 g, 100%, contains a minor amount of isomer) as an off-white solid; EI(+)-HRMS m/z calcd for C17H19ClN2O3 (M+) 334.1084, found 334.1083. Molecular Weight=334.8056; Exact Mass=334.1084

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: USRE046024E1uspto-grants-2016_06