تفاعل #3541
ord-6a90e5dbf8d9440f860586cc73a69716
معادلة التفاعل
المتفاعلات
الكواشف
ظروف التفاعل
المعالجة
- 1أخرىThe excess diethylaminoethylamine was removed in vacuo
- 2workup.DISSOLUTIONThe resulting oil was dissolved in diethyl ether
- 3workup.ADDITIONdiluted with hexane
- 4ترشيحfiltered
- 5workup.DISSOLUTIONThe resulting solid was dissolved in dichloromethane which
- 6غسيلwas washed several times with water
- 7تجفيفdried with magnesium sulfate
- 8تركيزconcentrated in vacuo
- 9أخرىThe residue was crystallized from ethyl acetate
الإجراء التجريبي
A mixture of 2,7-diamino-6-(2,6-dichlorophenyl)-pyrido[2,3-d]pyrimidine (4.0 g) from Example 1, sulfamic acid (2.53 g), and diethylaminoethylamine (40 mL) was heated to approximately 150° C. for 20 hours. The excess diethylaminoethylamine was removed in vacuo. The resulting oil was dissolved in diethyl ether, diluted with hexane, and then filtered. The resulting solid was dissolved in dichloromethane which was washed several times with water, dried with magnesium sulfate, and concentrated in vacuo. The residue was crystallized from ethyl acetate to give the title compound 6-(2,6-dichlorophenyl)-N2 -(2-diethylamino-ethyl)-pyrido[2,3-d]pyrimidine-2,7-diamine, CIMS (1% NH3 in CH4): 433=M+ +C2H5, 405=M+ +H, 389=M+ -Et, 360; mp 216°-219.5° C.