تفاعل #667699

ord-8b117dd8b5d44f5fb8586032ee787adf

معادلة التفاعل

O=C(O)c1cccc(C(F)(F)F)c1
3-trifluoromethylbenzoic acid
O=S(Cl)Cl
thionyl chloride
Nc1cnc2ccccc2c1N
3,4-diaminoquinoline
Nc1c(NC(=O)c2cccc(C(F)(F)F)c2)cnc2ccccc12
4-amino-3-(3-trifluoromethylbenzoylamino)quinoline
المردود 98.6%

الكواشف

لا شيء

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    workup.STIRRINGstirred at 0°-5° C. for 3 hours
  2. 2
    ترشيحThe resulting crystals are filtered
  3. 3
    غسيلwashed with water
  4. 4
    أخرىdried

الإجراء التجريبي

To a solution of 500 mg of 3-trifluoromethylbenzoic acid in 6 ml of anhydrous hexamethylphosphoramide (HMPA) and 0.6 ml of anhydrous acetonitrile is added dropwise 305 mg of thionyl chloride at -5°-0° C. under nitrogen. After stirring at the same temperature for 30 minutes, 380 mg of 3,4-diaminoquinoline is added and stirred at 0°-5° C. for 3 hours. The mixture is diluted with ice-water and neutralized with saturated aqueous sodium bicarbonate. The resulting crystals are filtered, washed with water, and dried to give 780 mg of 4-amino-3-(3-trifluoromethylbenzoylamino)quinoline B1 as a crude product. It is suspended in 15 g of polyphosphoric acid and heated at 120° C. for 4 hours with stirring. The mixture is poured into ice-water and neutralized with 1N sodium hydroxide. The resulting solid is filtered, washed with water and dried. It is chromatographed on silica gel with chloroform-methanol (10:1 v/v) as eluent, yielding 350 mg (47%) of C1 as colorless crystals.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US04753951uspto-grants-1988_06