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Bromine → 3-Bromo-7-chloroimidazo[1,2-a]pyridine

HRID 985523
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HRID 985523 반응식
[Cl:1][C:2]1[CH:7]=[CH:6][N:5]2[CH:8]=[CH:9][N:10]=[C:4]2[CH:3]=1.C([O-])(=O)C.[Na+].[Br:16]Br.C(=O)([O-])O.[Na+]>[Br-].[K+].CO>[Br:16][C:8]1[N:5]2[CH:6]=[CH:7][C:2]([Cl:1])=[CH:3][C:4]2=[N:10][CH:9]=1
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참가 물질

7

반응물 4

HCID 24408BromineHCID 516892Sodium BicarbonateHCID 517045Sodium AcetateHCID 196959017-Chloroimidazo(1,2-a)pyridine

생성물 1

HCID 467391183-Bromo-7-chloroimidazo[1,2-a]pyridine수율 80%

시약·촉매·용매 2

HCID 887Methanol용매
HCID 253877
Potassium Bromide
용매

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온도
0 °C

실험 절차

7-Chloroimidazo[1,2-α]pyridine (3.0 g, 19.7 mmol) and sodium acetate (1.94 g, 23.6 mmol) were dissolved in a saturated solution of potassium bromide in methanol (25 ml) and cooled to 0° C. before adding bromine (3.3 g, 20.7 mmol) dropwise over 5 min. The mixture was allowed to stir for 15 min before pouring onto saturated sodium hydrogencarbonate solution (200 ml). The resulting solid was collected by filtration and dried under high vacuum to give 3-bromo-7-chloroimidazo[1,2-α]pyridine (3.64 g, 80%) as a white solid. 1H NMR (360 MHz, CDCl3) δH 6.92 (1H, dd, J 2 and 7), 7.61 (1H, s), 7.63 (1H, d, J 2), 8.05 (1H, d, J 7).

후처리

  1. filtrationThe resulting solid was collected by filtration
  2. customdried under high vacuum

출처 및 근거

ORD 기록
ord-1f6bcddbd64b489a8c24ac9b26f2897d
출처 데이터셋
uspto-grants-2005_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06872731B2

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