Реакция #364603

Уравнение реакции

hydrochloric acid

1,8-diazabicyclo[5.4.0]undec-7-ene

Ethyl 3-amino-4,4,4-trifluorocrotonate

4-chloro-2-fluoro-5-methyl-6-nitro-N-phenoxycarbonylaniline

→

crude product

Выход 104.9%

3-(4-chloro-6-fluoro-3-methyl-2-nitrophenyl)-6-trifluoromethyl-2,4(1H, 3H)-pyrimidinedione

Выход 104.9%

Растворители

Water

dimethylformamide

dimethylformamide

Условия реакции

Обработка

1. 1
   workup.STIRRINGstirred for 0.5 hr
2. 2
   workup.STIRRINGby stirring at ambient temperature for 14 hr
3. 3
   ТемператураSolution was then heated to 80 ° C.
4. 4
   workup.STIRRINGstirred at this temperature for 4 hr
5. 5
   ЭкстракцияProduct was extracted with ethyl acetate
6. 6
   Другоеfollowed by evaporation of the solvent

Методика

Ethyl 3-amino-4,4,4-trifluorocrotonate (6.1 g, 33.1 mmol) was dissolved in dimethylformamide (47 ml) and stirred at −10 ° C. To this solution was slowly added 1,8-diazabicyclo[5.4.0]undec-7-ene (6.3 g, 41.4 mmol) and solution stirred for 0.5 hr. To this solution was slowly added a solution of 4-chloro-2-fluoro-5-methyl-6-nitro-N-phenoxycarbonylaniline (8.5 g) in dimethylformamide (25 ml) followed by stirring at ambient temperature for 14 hr. Solution was then heated to 80 ° C. and stirred at this temperature for 4 hr. Water was added and pH adjusted to 4 by addition of dilute hydrochloric acid. Product was extracted with ethyl acetate followed by evaporation of the solvent to afford the crude product (10.1 g) which was subjected to N-methylation as follows.

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