تفاعل #1779364

ord-255464e7c51f46f688e923fa60e16a09

معادلة التفاعل

Cc1cc(Cl)cc2c(=O)oc(=O)[nH]c12
6-chloro-8-methyl-2H-3,1-benzoxazine-2,4(1H)-dione
Cc1cc(Cl)cc2c(=O)oc(=O)[nH]c12
6-chloro-8-methyl-2H-3,1-benzoxazine-2,4(1H)-dione
Cc1cc(Cl)cc2c(=O)oc(=O)[nH]c12
6-chloro-8-methyl-2H-3,1-benzoxazine-2,4(1H)-dione
CCOC(C)=O
ethyl acetate
CC(=O)O
acetic acid
CN
methylamine
CNC(=O)c1cc(Cl)cc(C)c1N
title compound
المردود 95.6%
CNC(=O)c1cc(Cl)cc(C)c1N
2-Amino-5-chloro-N,3-dimethylbenzamide
المردود 95.6%

المذيبات

ظروف التفاعل

درجة الحرارة
37.5°CELSIUS
الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    أخرىA 300-mL flask equipped with a thermometer and nitrogen bubbler
  2. 2
    درجة الحرارةwas cooled
  3. 3
    درجة الحرارةto maintain the temperature below 35° C
  4. 4
    درجة الحرارةwas maintained at 40-45° C.
  5. 5
    workup.DISTILLATIONethyl acetate was distilled out at an internal temperature of about 46-60° C. and pressure of about 30 to 50 kPa
  6. 6
    أخرىremoved by distillation, water
  7. 7
    workup.ADDITIONwas added
  8. 8
    درجة الحرارةto maintain the original liquid volume in the reactor
  9. 9
    workup.DISTILLATIONto distill
  10. 10
    درجة الحرارةthe aqueous slurry was cooled to 10° C
  11. 11
    ترشيحThe solid was collected by filtration
  12. 12
    أخرىdried at 60° C.

الإجراء التجريبي

A 300-mL flask equipped with a thermometer and nitrogen bubbler was charged with ethyl acetate (100 mL) and 12.6 g (0.21 mol) of acetic acid. Anhydrous methylamine (6.3 g, 0.20 mol) was added below the surface of the liquid mixture, which was cooled to maintain the temperature below 35° C. Then 6-chloro-8-methyl-2H-3,1-benzoxazine-2,4(1H)-dione (21 g, 0.10 mol) (i.e. the product of Example 1) was added in portions while maintaining the reaction mixture at 35-40° C. After completion of the addition of the 6-chloro-8-methyl-2H-3,1-benzoxazine-2,4(1H)-dione the temperature was maintained at 40-45° C., and the progress of the reaction was monitored by HPLC analysis. After about 20 minutes, when no more than 0.5% 6-chloro-8-methyl-2H-3,1-benzoxazine-2,4(1H)-dione remained, water (50 mL) was added. A distillation head was attached, moderate vacuum was applied, and ethyl acetate was distilled out at an internal temperature of about 46-60° C. and pressure of about 30 to 50 kPa. To replace the ethyl acetate removed by distillation, water was added to maintain the original liquid volume in the reactor. When a significant amount of water began to distill, the aqueous slurry was cooled to 10° C. The solid was collected by filtration and dried at 60° C. and 13.3 kPa to afford the title compound as a white crystalline solid (19 g, ca. 95% yield, >98% purity by peak area in HPLC analysis).

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US08153844B2uspto-grants-2012_04