Reacción #562641

Ecuación de reacción

2-amino-3-methyl-5-chlorobenzoic acid

methanesulfonyl chloride

product

3-Chloro-1-(3-chloro-2-pyridinyl)-1H-pyrazole-5-carboxylic acid

triethylamine

triethylamine

methanesulfonyl chloride

→

title product

Rendimiento 38.4%

6-Chloro-2-[3-chloro-1-(3-chloro-2-pyridinyl)-1H-pyrazol-5-yl]-8-methyl-4H-3,1-benzoxazin-4-one

Rendimiento 38.4%

Disolventes

acetonitrile

acetonitrile

acetonitrile

Condiciones de reacción

Tratamiento posterior

1. 1
   workup.ADDITIONa mixture of the carboxylic
2. 2
   workup.STIRRINGstirring
3. 3
   workup.WAITwas continued for an additional 10 minutes
4. 4
   Otrothe temperature below 10° C
5. 5
   workup.STIRRINGThe reaction mixture was stirred 60 minutes at 0° C.
6. 6
   TemperaturaThe reaction mixture was then warmed to room temperature
7. 7
   workup.STIRRINGstirred for an additional 2 hours
8. 8
   ConcentraciónThe reaction mixture was then concentrated
9. 9
   Otrothe crude product was chromatographed on silica gel

Procedimiento

To a solution of methanesulfonyl chloride (6.96 g, 61.06 mmol) in acetonitrile (150 mL) was added dropwise a mixture of the carboxylic add product from Step D (15.0 g, 58.16 mmol) and triethylamine (5.88 g, 58.16 mmol) in acetonitrile (150 mL) at −5° C. The reaction mixture was then stirred for 30 minutes at 0° C. Then, 2-amino-3-methyl-5-chlorobenzoic acid from Example 6, Step A (10.79 g, 58.16 mmol) was added, and stirring was continued for an additional 10 minutes. A solution of triethylamine (11.77 g, 116.5 mmol) in acetonitrile was then added dropwise while keeping the temperature below 10° C. The reaction mixture was stirred 60 minutes at 0° C., and then methanesulfonyl chloride (6.96 g, 61.06 mmol) was added. The reaction mixture was then warmed to room temperature and stirred for an additional 2 hours. The reaction mixture was then concentrated, and the crude product was chromatographed on silica gel using methylene chloride as eluent to afford the title product as a yellow solid (9.1 g).

Fuente