تفاعل #939050

ord-7dabf0aa854348f689c2c225cf01be77

معادلة التفاعل

COC(=O)C1(c2ccc(OCC(C)C)c(C#N)c2)Nc2ccccc2S1
Methyl 2-(3-cyano-4-isobutyloxyphenyl)-1,3-benzothiazole-carboxylate
C1CCOC1.CCO.CO
methanol ethanol THF
[K+].[OH-]
potassium hydroxide
Cl
hydrochloric acid
CC(C)COc1ccc(-c2nc3cccc(C(=O)O)c3s2)cc1C#N
desired compound
المردود 83.0%
CC(C)COc1ccc(-c2nc3cccc(C(=O)O)c3s2)cc1C#N
2-(3-Cyano-4-isobutyloxyphenyl)-1,3-benzothiazole-7-carboxylic acid
المردود 83.0%

المذيبات

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    workup.DISTILLATIONto distill the solvent off
  2. 2
    استخلاصThe residue was extracted with chloroform
  3. 3
    تجفيفThe chloroform portion was then dried over anhydrous magnesium sulfate
  4. 4
    workup.DISTILLATIONtoo distill the solvent off
  5. 5
    أخرىThe residual crystalline product was recrystallized from toluene

الإجراء التجريبي

Methyl 2-(3-cyano-4-isobutyloxyphenyl)-1,3-benzothiazole-carboxylate (288 mg, 0.786 mmol) was dissolved in a mixed solvent (50 mL) of methanol/ethanol/THF (2/1/2), and, then a solution of potassium hydroxide (281 mg, 5 mmol) in water (10 mL) was added and stirred for one hour at room temperature. The mixture was made acidic by addition of aqueous 1M hydrochloric acid, and placed under reduced pressure to distill the solvent off. The residue was extracted with chloroform. The chloroform portion was then dried over anhydrous magnesium sulfate and placed under reduced pressure too distill the solvent off. The residual crystalline product was recrystallized from toluene, to give 230 mg (yield 83%) of the desired compound in the form of a white crystalline product.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US07253154B2uspto-grants-2007_08