Реакция #792157

Уравнение реакции

benzoxazinone

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

isopropylamine

diethyl ether

→

title compound

Выход 87.3%

1-(3-Chloro-2-pyridinyl)-N-[2-methyl-6-[[(1-methylethyl)-amino]carbonyl]phenyl]-3-(trifluoromethyl)-1H-pyrazole-5-carboxamide

Выход 87.3%

Растворители

dichloromethane

Условия реакции

Обработка

1. 1
   workup.ADDITIONthe suspension thinned during the addition
2. 2
   ТемператураThe reaction mixture was then warmed
3. 3
   Температураto reflux for 1.5 h
4. 4
   ДругоеA new suspension formed
5. 5
   ДругоеThe solids were collected
6. 6
   Промывкаwashed with ether
7. 7
   ДругоеThe solids were air-dried
8. 8
   Другоеdried in vacuo at 90° C. for 5 h

Методика

To a suspension of the benzoxazinone product of Step D (124 g, 300 mmol) in dichloromethane (500 mL) was added dropwise isopropylamine (76 mL, 900 mmol) at room temperature. The temperature of the reaction mixture rose and the suspension thinned during the addition. The reaction mixture was then warmed to reflux for 1.5 h. A new suspension formed. The reaction mixture was cooled to room temperature and diethyl ether (1.3 L) was added and the mixture stirred at room temperature overnight. The solids were collected and washed with ether. The solids were air-dried and then dried in vacuo at 90° C. for 5 h to yield 122 g of the title compound, a compound of the present invention, as a fluffy white solid, melting at 194-196° C.

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