تفاعل #40364
ord-7ccb126b89ca40838648d5c99efc243b
معادلة التفاعل
المتفاعلات
الكواشف
لا شيء
ظروف التفاعل
الظروف التفصيلية
See reaction.notes.procedure_details.
المعالجة
- 1workup.ADDITIONwas added
- 2درجة الحرارةThe reaction mixture was refluxed for 20 hrs
- 3تركيزThe reaction mixture was concentrated in vacuo
- 4workup.ADDITIONdiluted with ethyl acetate
- 5غسيلwashed with water
- 6تجفيفThe organic layer was dried over magnesium sulfate
- 7تركيزconcentrated in vacuo
- 8أخرىyielded 220 mg (59%) with a purity of 72% log P (pH=2.3)=1.45
الإجراء التجريبي
To a mixture of 310 mg (0.8 mmol) of 4-[(2-chloro-6-methylpyrimidin-4-yl)oxy]-2,5-dimethyl-aniline in 20 ml acetonitrile 208 mg (1.5 mmol) of N-(dimethoxymethyl)-N-methylethanamine (77% pure) was added. The reaction mixture was refluxed for 20 hrs. The reaction mixture was concentrated in vacuo, diluted with ethyl acetate and washed with water. The organic layer was dried over magnesium sulfate and concentrated in vacuo yielded 220 mg (59%) with a purity of 72% log P (pH=2.3)=1.45.