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HCID 57786383, Verbindung → HCID 57785846, Verbindung

HRID 1399257
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Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 1399257
[CH2:1]([Zn]CC)C.[Cl:6][C:7]1[C:15]2[N:14]=[C:13]3[N:16]([C:20]4[C:25]([CH3:26])=[CH:24][C:23]([Cl:27])=[CH:22][C:21]=4[Cl:28])[CH2:17][CH2:18][CH2:19][N:12]3[C:11]=2[C:10]([CH:29]([OH:33])[CH2:30][CH:31]=[CH2:32])=[CH:9][CH:8]=1>ClCCl.[Cl-].[NH4+]>[Cl:6][C:7]1[C:15]2[N:14]=[C:13]3[N:16]([C:20]4[C:25]([CH3:26])=[CH:24][C:23]([Cl:27])=[CH:22][C:21]=4[Cl:28])[CH2:17][CH2:18][CH2:19][N:12]3[C:11]=2[C:10]([CH:29]([OH:33])[CH2:30][CH:31]2[CH2:1][CH2:32]2)=[CH:9][CH:8]=1
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Komponenten

5

Edukt 2

HCID 57786383HCID 57786383, VerbindungHCID 178418750HCID 178418750, Verbindung

Produkt 1

HCID 57785846HCID 57785846, VerbindungAusbeute 34,1 %

Reagenzien, Katalysatoren, Lösungsmittel 2

HCID 6344DichloromethaneLösungsmittelHCID 25517Ammonium ChlorideLösungsmittel

Versuchsvorschrift

Under nitrogen atmosphere, diethyl zinc (1 M solution in hexane, 0.800 mL, 0.800 mmol) was added to a solution of 1-[9-chloro-1-(2,4-dichloro-6-methylphenyl)-1,2,3,4-tetrahydropyrimido[1,2-a]benzimidazol-6-yl]but-3-en-1-ol (70.0 mg, 0.160 mmol) in dichloromethane (3.2 mL) at 0° C., and then diiodemethane (0.129 mL, 1.60 mmol) was added at 0° C. The resultant mixture was stirred at room temperature for 2 hr, diluted with aqueous saturated ammonium chloride, and extracted with ethyl acetate. The combined organic layer was washed with brine, dried over anhydrous sodium sulfate, filtered and concentrated in vacuo. The residue was purified by flash column chromatography on silica gel eluting with a 20-50% ethyl acetate/n-hexane gradient mixture to give a solid, which was recrystallized from ethyl acetate/hexane to afford the title compound as a colorless solid (24.6 mg, 00540 mmol, 34%).

Aufarbeitung

  1. additiondiiodemethane (0.129 mL, 1.60 mmol) was added at 0° C
  2. extractionextracted with ethyl acetate
  3. washThe combined organic layer was washed with brine
  4. dry with materialdried over anhydrous sodium sulfate
  5. filtrationfiltered
  6. concentrationconcentrated in vacuo
  7. customThe residue was purified by flash column chromatography on silica gel eluting with a 20-50% ethyl acetate/n-hexane gradient mixture
  8. customto give a solid, which
  9. customwas recrystallized from ethyl acetate/hexane

Quellen und Nachweise

ORD-Eintrag
ord-77fd8fb92eeb4759bd6fe6ce5f93b693
Quelldatensatz
uspto-grants-2014_12
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US08901141B2

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