Hydrochloric Acid → 2-Chloro-6-propylimidazo[1,2-b]pyridazine

HRID 969725

반응식

HRID 969725 반응식
[Cl:1][C:2]1[N:3]=[C:4]2[CH:9]=[CH:8][C:7](Cl)=[N:6][N:5]2[CH:11]=1.O1C[CH2:15][CH2:14][CH2:13]1.C([Mg]Br)CC.Cl>Cl[Ni](Cl)([P](C1C=CC=CC=1)(C1C=CC=CC=1)C1C=CC=CC=1)[P](C1C=CC=CC=1)(C1C=CC=CC=1)C1C=CC=CC=1.O>[Cl:1][C:2]1[N:3]=[C:4]2[CH:9]=[CH:8][C:7]([CH2:13][CH2:14][CH3:15])=[N:6][N:5]2[CH:11]=1

참가 물질

7

반응물 4

HCID 313Hydrochloric AcidHCID 8028Tetrahydrofuran2회HCID 144223582,6-Dichloroimidazo[1,2-b]pyridazineHCID 178455851HCID 178455851, 화합물

생성물 1

HCID 230280952-Chloro-6-propylimidazo[1,2-b]pyridazine

시약·촉매·용매 2

HCID 178418751HCID 178418751, 화합물촉매HCID 962Water용매

실험 절차

2,6-Dichloroimidazo[1,2-b]pyridazine (0.50 g, 2.66 mmol) and bis(triphenylphosphine)nickel(II) dichloride (0.17 g, 0.27 mmol) were added to tetrahydrofuran (5.0 ml) under a nitrogen stream, and a solution of n-propylmagnesium bromide in tetrahydrofuran (2 M, 1.99 ml, 3.99 mmol) was added dropwise over 10 minutes to the mixture under ice-cooling. The mixture was stirred for 10 minutes under ice-cooling, and the reaction mixture was warmed to room temperature and stirred for 4 hours at room temperature. Cold water (50 ml) was added to the reaction mixture which was then acidified with dilute hydrochloric acid, and extracted with ethyl acetate. The extracts were washed with dilute hydrochloric acid, a saturated saline, an aqueous saturated sodium bicarbonate solution and a saturated saline in this order. The resulting organic layer was dried over anhydrous magnesium sulfate, filtrated and concentrated. The concentrated residue was purified by silica gel column chromatography (ethyl acetate:hexane=3:7) to give the title compound as white crystals. The yield was 0.21 g (40.4%).

후처리

  1. temperaturecooling
  2. temperaturecooling
  3. stirringstirred for 4 hours at room temperature
  4. extractionextracted with ethyl acetate
  5. washThe extracts were washed with dilute hydrochloric acid
  6. dry with materialThe resulting organic layer was dried over anhydrous magnesium sulfate
  7. filtrationfiltrated
  8. concentrationconcentrated
  9. customThe concentrated residue was purified by silica gel column chromatography (ethyl acetate:hexane=3:7)

출처 및 근거

ORD 기록
ord-e14f86c975634133a60984a37f97b59a
출처 데이터셋
uspto-grants-2007_12
특허 번호
US07307165B2

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