Реакция #90237

Уравнение реакции

Methanesulfonyl chloride

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

pyrazolecarboxylic acid

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

pyridine

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

product

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

pyridine

methanesulfonyl chloride

→

title product

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

Растворители

acetonitrile

acetonitrile

acetonitrile

acetonitrile

Water

Условия реакции

Обработка

1. 1
   ДругоеA slurry formed during the addition
2. 2
   workup.ADDITIONwas added
3. 3
   Промывкаrinsing with more acetonitrile (5 mL)
4. 4
   workup.STIRRINGThe mixture was stirred 15 minutes at −5 to 0° C.
5. 5
   workup.STIRRINGThe reaction mixture was stirred 15 minutes more at this temperature
6. 6
   Температураto warm slowly to room temperature
7. 7
   workup.STIRRINGstirred 4 h
8. 8
   workup.STIRRINGthe mixture was stirred 15 minutes
9. 9
   ФильтрацияThen the mixture was filtered
10. 10
    Промывкаthe solids were washed with 2:1 acetonitrile-water (3×3 mL)
11. 11
    Сушкаwith acetonitrile (2×3 mL), and dried under nitrogen

Методика

Methanesulfonyl chloride (1.0 mL, 1.5 g, 13 mmol) was dissolved in acetonitrile (10 mL), and the mixture was cooled to −5° C. A solution of 3-bromo-1-(3-chloro-2-pyridinyl)-1H-pyrazole-5-carboxylic acid (i.e. the pyrazolecarboxylic acid product of Example 5, Step D) (3.02 g, 10 mmol) and pyridine (1.4 mL, 1.4 g, 17 mmol) in acetonitrile (10 mL) was added dropwise over 5 minutes at −5 to 0° C. A slurry formed during the addition. The mixture was stirred 5 minutes at this temperature, and then a mixture of 2-amino-3-methyl-5-chlorobenzoic acid (i.e. the product of Example 1 Step A) (1.86 g, 10 mmol) and pyridine (2.8 mL, 2.7 g, 35 mmol) in acetonitrile (10 mL) was added, rinsing with more acetonitrile (5 mL). The mixture was stirred 15 minutes at −5 to 0° C., and then methanesulfonyl chloride (1.0 mL, 1.5 mL, 13 mmol) in acetonitrile (5 mL) was added dropwise over 5 minutes at a temperature of −5 to 0° C. The reaction mixture was stirred 15 minutes more at this temperature, then allowed to warm slowly to room temperature, and stirred 4 h. Water (20 mL) was added dropwise, and the mixture was stirred 15 minutes. Then the mixture was filtered, and the solids were washed with 2:1 acetonitrile-water (3×3 mL), then with acetonitrile (2×3 mL), and dried under nitrogen to afford the title product as a light yellow powder, 4.07 g (90.2% crude yield), melting at 203-205° C. HPLC of the product using a Zorbax® RX-C8 chromatography column (4.6 mm×25 cm, eluent 25-95% acetonitrile/pH 3 water) showed a major peak corresponding to the title compound and having 95.7% of total chromatogram peak area.

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