تفاعل #2186199
ord-39f8254b148440e5a54cc71bd189ff02
معادلة التفاعل
2-Amino-5-chloropyridine
4-chloro-3-oxo-butyric acid methyl ester
→
desired product
المردود 31.0%
(6-Chloro-imidazo[1,2-a]pyridin-2-yl)-acetic acid methyl ester
المردود 31.0%
الكواشف
لا شيء
المذيبات
ظروف التفاعل
الظروف التفصيلية
See reaction.notes.procedure_details.
المعالجة
- 1أخرىThe resulting brown suspension is evaporated
- 2درجة الحرارةheated 1 h to 90° C. under high vacuum
- 3أخرىThe organic phase is then separated
- 4أخرىevaporated
- 5أخرىto yield a brownish solid
- 6أخرىchromatographed (silica gel, ethyl acetate/petroleum ether 4:1)
الإجراء التجريبي
1.28 g (10 mmol) 2-Amino-5-chloropyridine and 1.18 mL (1 eq) 4-chloro-3-oxo-butyric acid methyl ester are heated to 115° C. in 15 mL toluene for 18 h. The resulting brown suspension is evaporated and heated 1 h to 90° C. under high vacuum, then cooled to room temperature and stirred in 100 mL dichloromethane, 10 mL saturated aqueous sodium bicarbonate solution and 40 mL water at 0° C. for one hour. The organic phase is then separated and evaporated to yield a brownish solid that is column chromatographed (silica gel, ethyl acetate/petroleum ether 4:1) to yield 700 mg (31 %) desired product as a beige powder. MS(EI+): 225-227 (M+1).