تفاعل #667701

ord-50d0b5596cc24c4487e3a777096879c7

معادلة التفاعل

Cc1ncoc1C(=O)O
4-methyloxazole-5-carboxylic acid
O=S(Cl)Cl
thionyl chloride
CN(C)P(=O)(N(C)C)N(C)C
hexamethylphosphoramide
Nc1cnc2ccccc2c1N
3,4-diaminoquinoline
Cc1cnoc1C(=O)Nc1cnc2ccccc2c1N
4-amino-3-(4-methylisoxazole-5-ylcarbonylamino)quinoline

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 solid is filtered
  3. 3
    غسيلwashed with water

الإجراء التجريبي

To a solution of 300 mg of 4-methyloxazole-5-carboxylic acid in 4 ml of hexamethylphosphoramide and 0.4 ml of acetonitrile is added 268 mg of thionyl chloride at -5°-0° C. under nitrogen. After stirring at the same temperature for 30 minutes, 340 mg of 3,4-diaminoquinoline A1 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 solid is filtered and washed with water to give 425 mg of 4-amino-3-(4-methylisoxazole-5-ylcarbonylamino)quinoline as crude crystals. It is suspended in 12 ml of Dowtherm A (Dow Chemimical Co.) and refluxed for 2.5 hours. The cooled mixture is diluted with 50 ml of n-hexane and the resulting solid is collected by filtration. It is chromatographed on silica gel with dichloromethane-methanol (20:1 v/v) as eluent to yield a crude solid which is recrystallized from ethyl acetate-methanol, giving 297 mg of C99 as pale yellow crystals.

المصدر

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