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Hydrochloric Acid → 8-Amino-6-(2,4-dichloro-phenyl)-imidazo[1,2-a]pyridine-7-carbonitrile

HRID 420514
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HRID 420514 반응식
[N:1]([C:4]1[C:5]2[N:6]([CH:20]=[CH:21][N:22]=2)[CH:7]=[C:8]([C:12]2[CH:17]=[CH:16][C:15]([Cl:18])=[CH:14][C:13]=2[Cl:19])[C:9]=1[C:10]#[N:11])=[N+]=[N-].C1(P(C2C=CC=CC=2)C2C=CC=CC=2)C=CC=CC=1.Cl>CO.O>[NH2:1][C:4]1[C:5]2[N:6]([CH:20]=[CH:21][N:22]=2)[CH:7]=[C:8]([C:12]2[CH:17]=[CH:16][C:15]([Cl:18])=[CH:14][C:13]=2[Cl:19])[C:9]=1[C:10]#[N:11]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 3

HCID 313Hydrochloric AcidHCID 11776TriphenylphosphineHCID 86634890HCID 86634890, 화합물

생성물 1

HCID 666590048-Amino-6-(2,4-dichloro-phenyl)-imidazo[1,2-a]pyridine-7-carbonitrile수율 52.4%

시약·촉매·용매 2

HCID 887Methanol용매HCID 962Water
용매

실험 절차

A mixture of crude 8-azido-6-(2,4-dichloro-phenyl)-imidazo[1,2-a]pyridine-7-carbonitrile (68 mg, 0.21 mmol) and triphenylphosphine (83.7 mg, 0.32 mmol) in MeOH (2.5 mL) was stirred and refluxed for 1 h. 2 M HCl in water (1 mL) was added and the reaction mixture was further refluxed for 1 h. The reaction mixture was cooled to RT, concentrated under vacuum and the remaining residue was dissolved in water. The aqueous solution was basified to pH 12 by the addition of 2 M NaOH in water. The resulting slurry was extracted with DCM (2×) and the combined organic fractions were dried over Na2SO4, filtered and evaporated. The remaining residue was dissolved in hot MeOH, then the solution was slowly cooled to RT and the formed precipitate was filtered and washed with cold MeOH to yield the title compound (32.5 mg, 0.11 mmol, 52%) as a brownish solid. MS: 303 [M+1]+; HPLC: AtRet=1.72.

후처리

  1. temperaturerefluxed for 1 h
  2. temperaturethe reaction mixture was further refluxed for 1 h
  3. concentrationconcentrated under vacuum
  4. dissolutionthe remaining residue was dissolved in water
  5. additionThe aqueous solution was basified to pH 12 by the addition of 2 M NaOH in water
  6. extractionThe resulting slurry was extracted with DCM (2×)
  7. dry with materialthe combined organic fractions were dried over Na2SO4
  8. filtrationfiltered
  9. customevaporated
  10. dissolutionThe remaining residue was dissolved in hot MeOH
  11. temperaturethe solution was slowly cooled to RT
  12. filtrationthe formed precipitate was filtered
  13. washwashed with cold MeOH

출처 및 근거

ORD 기록
ord-a566f4a363b14e3380de5074e877e9b5
출처 데이터셋
uspto-grants-2012_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08097617B2

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