تفاعل #710477
ord-e0110b7b7b7a4c6ba457b86c8afcb6fd
معادلة التفاعل
المتفاعلات
الكواشف
المذيبات
ظروف التفاعل
المعالجة
- 1أخرىthe reaction and liquid separation
- 2غسيلThe organic layer was washed once with water and twice with 1% hydrochloric acid
- 3تجفيفdried over anhydrous magnesium sulfate
- 4تركيزconcentrated under reduced pressure
- 5workup.ADDITIONDiethyl ether was added
- 6أخرىto precipitate a solid
- 7أخرىthus the solid was collected
- 8أخرىdried
- 9أخرىto obtain the subject material
- 10أخرىAmount obtained 61 mg (yield 62%)
الإجراء التجريبي
70 mg (0.27 mmol) of the 1-[(6-chloropyridin-3-yl)methyl]pyridin-2(1H)-imine hydrochloride obtained by the method described in another method of Synthetic Example P1 was dissolved in 4 ml of anhydrous dichloromethane, 94 μl (0.68 mmol, 68 mg) of triethylamine and 33 g (0.27 mmol, 49 mg) of trichloroacetyl chloride were added thereto in sequence, and the resulting mixture was stirred at room temperature for 1 hour. After the reaction was completed, water was added thereto to stop the reaction and liquid separation was performed with dichloromethane and water. The organic layer was washed once with water and twice with 1% hydrochloric acid, dried over anhydrous magnesium sulfate and concentrated under reduced pressure. Diethyl ether was added thereto to precipitate a solid, and thus the solid was collected and dried to obtain the subject material. Amount obtained 61 mg (yield 62%).