반응 #2186199

ord-39f8254b148440e5a54cc71bd189ff02

반응 방정식

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
수율 31.0%
COC(=O)Cc1cn2cc(Cl)ccc2n1
(6-Chloro-imidazo[1,2-a]pyridin-2-yl)-acetic acid methyl ester
수율 31.0%

용매

반응 조건

상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    기타The resulting brown suspension is evaporated
  2. 2
    온도heated 1 h to 90° C. under high vacuum
  3. 3
    기타The organic phase is then separated
  4. 4
    기타evaporated
  5. 5
    기타to yield a brownish solid
  6. 6
    기타chromatographed (silica gel, ethyl acetate/petroleum ether 4:1)

실험 절차

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).

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US07569337B2uspto-grants-2009_08