Реакция #10342
ord-74338b5aed30449facdcc0ace8215f09
Уравнение реакции
Реактанты
Реагенты
Условия реакции
Обработка
- 1Другоеprepared from the product
- 2Другоеfollowed by evaporation of the solvent]
- 3workup.ADDITIONthen poured onto water (500 ml) and diethylether (250 ml)
- 4workup.ADDITIONwas added
- 5workup.STIRRINGthe solution was stirred for 30 min
- 6ДругоеThe layers were separated
- 7Температураcooled to 0° C. for 1 h
- 8ФильтрацияThe precipitated product was filtered off
- 9Промывкаwashed with water and diethylether
- 10Другоеdried
Методика
To 4,6-dichloro-5-p-tolyl-pyrimidine (Referential Example 7) (2.0 g) dissolved in DMSO (35 ml) was added di-isopropyl-ethyl-amine (1.46 ml) followed by addition of 4-methyl-phenyl sulfamic acid amide potassium salt (2.78 g) [prepared from the product described in Referential Example 19 and potassium tert.-butylate in methanol followed by evaporation of the solvent]. The mixture was stirred for 48 h at rt then poured onto water (500 ml) and diethylether (250 ml) was added and the solution was stirred for 30 min. The layers were separated and the water layer was acidified with acetic acid (2.0 ml) and cooled to 0° C. for 1 h. The precipitated product was filtered off and washed with water and diethylether and dried to give 4-methyl-phenyl sulfamic acid-[6-chloro-5-(p-tolyl)-4-pyrimidinyl]-amide (2.02 g). tR=5.00 min (LC); [M+H]+=389.11 (ES+);