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2-Methyl-2-butene → 6-Chloroimidazo[1,2-b]pyridazine-3-carboxylic acid

HRID 870767
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HRID 870767 반응식
[Cl:1][C:2]1[CH:3]=[CH:4][C:5]2[N:6]([C:8]([CH:11]=[O:12])=[CH:9][N:10]=2)[N:7]=1.CC(=CC)C.Cl([O-])=[O:19].[Na+]>CC(O)(C)C.C1COCC1.O>[Cl:1][C:2]1[CH:3]=[CH:4][C:5]2[N:6]([C:8]([C:11]([OH:19])=[O:12])=[CH:9][N:10]=2)[N:7]=1
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참가 물질

7

반응물 3

HCID 105532-Methyl-2-buteneHCID 114467026-Chloroimidazo[1,2-b]pyridazine-3-carbaldehydeHCID 23668197Sodium Chlorite

생성물 1

HCID 567666386-Chloroimidazo[1,2-b]pyridazine-3-carboxylic acid수율 67%

시약·촉매·용매 3

HCID 962Water용매HCID 6386tert-Butanol
용매
HCID 8028Tetrahydrofuran용매

실험 절차

To a solution of 6-chloroimidazo[1,2-b]pyridazine-3-carbaldehyde (1.82 g, 10 mmol), in t-BuOH (90 mL) and 2-methyl-2-butene in THF (30 mL, 2.0 M) was added a solution of sodium chlorite (80%, 9.0 g, 100 mmol) and NaH2PO4 (1 g, 8 mmol) in water (45 mL). The mixture was stirred at rt for overnight, concentrated, diluted with water, acidified to PH=4, precipitated white solid, filtered to give 6-chloroimidazo[1,2-b]pyridazine-3-carboxylic acid as white solid (1.2 g, 67% yield)). 1H NMR (400 MHz, DMSO-d6) δ ppm 8.29 (d, J=9.60 Hz, 1H), 8.22 (s, 1H), 7.50 (d, J=9.60 Hz, 1H); LRMS (ESI) m/e 198.1 [(M+H)+, calcd for C7H6ClN3O2 198.6].

후처리

  1. concentrationconcentrated
  2. additiondiluted with water
  3. customprecipitated white solid
  4. filtrationfiltered

출처 및 근거

ORD 기록
ord-d69045a8298a407c8d4812ac994582ae
출처 데이터셋
uspto-grants-2015_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08969565B2

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