تفاعل #939042

ord-9e24bb7848254180b2bbc667eb2be13d

معادلة التفاعل

CC(=O)OCc1c2ccccc2c(COC(C)=O)c2ccccc12
acetic
Nc1ncnc(O)c1N
4,5-Diamino-6-hydroxypyrimidine
O=C([O-])O.[Na+]
sodium hydrogen carbonate
CC(C)COc1ccc(C(=O)Cl)cc1[N+](=O)[O-]
4-isobutoxy-3-nitrobenzoyl chloride
Cl
hydrochloric acid
CC(C)COc1ccc(C(=O)Nc2c(N)ccnc2O)cc1[N+](=O)[O-]
desired compound
المردود 69.0%
CC(C)COc1ccc(C(=O)Nc2c(N)ccnc2O)cc1[N+](=O)[O-]
4-Amino-6-hydroxy-5-(4-isobutoxy-3-nitrobenzoyl)aminopyridine
المردود 69.0%

المذيبات

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    درجة الحرارةunder cooling with ice
  2. 2
    درجة الحرارةunder cooling with ice
  3. 3
    أخرىplaced under reduced pressure at room temperature
  4. 4
    workup.DISTILLATIONto distill ethyl acetate off, and
  5. 5
    workup.STIRRINGstirred for 30 min. at room temperature
  6. 6
    ترشيحThe precipitated solid product was collected by filtration
  7. 7
    غسيلwashed successively with water and diethyl ether
  8. 8
    أخرىdried successively in air and reduced pressure

الإجراء التجريبي

4,5-Diamino-6-hydroxypyrimidine (527 mg, 4.18 mmol) was added to an aqueous suspension of sodium hydrogen carbonate (3.15 g, 41.8 mmol) in water (10 mL) under cooling with ice. Subsequently, a solution of 4-isobutoxy-3-nitrobenzoyl chloride (1.08 g, 4.18 mmol) in ethyl acetate (10 mL) was added. The resulting mixture was stirred for 3 hours under cooling with ice, made acetic by addition of 6 M hydrochloric acid, placed under reduced pressure at room temperature to distill ethyl acetate off, and stirred for 30 min. at room temperature. The precipitated solid product was collected by filtration, washed successively with water and diethyl ether, and dried successively in air and reduced pressure, to give 963 mg (yield 69%) of the desired compound in the form of a powdery product.

المصدر

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