Реакция #3513

Уравнение реакции

charcoal

t-butyl isocyanate

7-amino-6-(2,6-dichlorophenyl)-2-(3-diethylamino-propylamino)-pyrido[2,3-d]pyrimidine

sodium hydride

→

1-tert-butyl-3-[6-(2,6-dichlorophenyl)-2-(3-diethylamino-propylamino)-pyrido[2,3-d]pyrimidin-7-yl]-urea

Выход 27.9%

Растворители

water

DMF

Условия реакции

Обработка

1. 1
   workup.STIRRINGthe mixture was stirred for 18 hours
2. 2
   Фильтрацияthe insoluble material was collected by filtration
3. 3
   Другоеto form a solution
4. 4
   Фильтрацияthe suspension filtered through celite
5. 5
   Промывкаwashing with water
6. 6
   Фильтрацияthe insoluble product was collected by filtration
7. 7
   Промывкаwashed with water
8. 8
   ДругоеA 180-mg sample of the product was further purified by reverse phase preparative HPLC on a C18 reverse phase column
9. 9
   Промывкаeluting with a solvent gradient
10. 10
    workup.WAITstarting from 86% of 0.1% trifluoroacetic acid in water/14% acetonitrile to 14% of 0.1% trifluoroacetic acid in water/86% acetonitrile over a 22-minute

Методика

To a solution of 7-amino-6-(2,6-dichlorophenyl)-2-(3-diethylamino-propylamino)-pyrido[2,3-d]pyrimidine (0.48 g) from Example 20 in DMF (5 mL) was added 60% sodium hydride suspension (46 mg), and the mixture was stirred for 1 hour at room temperature. To the reaction mixture was added t-butyl isocyanate (0.113 g), and the mixture was stirred for 18 hours. The reaction mixture was diluted with water and the insoluble material was collected by filtration. The solid was suspended in water (20 mL) and acidified with 1.0N HCl to form a solution. Activated charcoal was added to the solution, and the suspension filtered through celite, washing with water. The filtrate was made basic with 1.0N NaOH, and the insoluble product was collected by filtration and washed with water. A 180-mg sample of the product was further purified by reverse phase preparative HPLC on a C18 reverse phase column, eluting with a solvent gradient starting from 86% of 0.1% trifluoroacetic acid in water/14% acetonitrile to 14% of 0.1% trifluoroacetic acid in water/86% acetonitrile over a 22-minute time period to afford 165 mg of 1-tert-butyl-3-[6-(2,6-dichlorophenyl)-2-(3-diethylamino-propylamino)-pyrido[2,3-d]pyrimidin-7-yl]-urea, mp dec >80° C.

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