تفاعل #2186199

ord-39f8254b148440e5a54cc71bd189ff02

معادلة التفاعل

Nc1ccc(Cl)cn1
2-Amino-5-chloropyridine
COC(=O)CC(=O)CCl
4-chloro-3-oxo-butyric acid methyl ester
COC(=O)Cc1cn2cc(Cl)ccc2n1
desired product
المردود 31.0%
COC(=O)Cc1cn2cc(Cl)ccc2n1
(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

  1. 1
    أخرىThe resulting brown suspension is evaporated
  2. 2
    درجة الحرارةheated 1 h to 90° C. under high vacuum
  3. 3
    أخرىThe organic phase is then separated
  4. 4
    أخرىevaporated
  5. 5
    أخرىto yield a brownish solid
  6. 6
    أخرىchromatographed (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).

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US07569337B2uspto-grants-2009_08