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Diisopropylethylamine → HCID 11598307, Verbindung

HRID 2099367
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Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 2099367
Cl.[CH3:2][N:3]([CH2:5][C:6](Cl)=[O:7])[CH3:4].Cl.Cl.[Cl:11][C:12]1[C:13]([F:38])=[C:14]([NH:18][C:19]2[C:28]3[C:23](=[CH:24][C:25]([O:31][CH:32]4[CH2:37][CH2:36][NH:35][CH2:34][CH2:33]4)=[C:26]([O:29][CH3:30])[CH:27]=3)[N:22]=[CH:21][N:20]=2)[CH:15]=[CH:16][CH:17]=1.C(N(C(C)C)CC)(C)C>C(Cl)Cl>[Cl:11][C:12]1[C:13]([F:38])=[C:14]([NH:18][C:19]2[C:28]3[C:23](=[CH:24][C:25]([O:31][CH:32]4[CH2:37][CH2:36][N:35]([C:6](=[O:7])[CH2:5][N:3]([CH3:4])[CH3:2])[CH2:34][CH2:33]4)=[C:26]([O:29][CH3:30])[CH:27]=3)[N:22]=[CH:21][N:20]=2)[CH:15]=[CH:16][CH:17]=1
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

5

Edukt 3

HCID 81531DiisopropylethylamineHCID 139949912-(Dimethylamino)acetyl chloride hydrochlorideHCID 67415388HCID 67415388, Verbindung

Produkt 1

HCID 11598307HCID 11598307, VerbindungAusbeute 45 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 6344DichloromethaneLösungsmittel

Versuchsvorschrift

N,N-Dimethylaminoacetyl chloride hydrochloride (100 mg) was added portionwise to a stirred solution of N-(3-chloro-2-fluorophenyl)-6-methoxy-7-(piperidin-4-yloxy)quinazolin-4-amine dihydrochloride (250 mg, 0.57 mmol) and diisopropylethylamine (300 μl) in methylene chloride (25 ml) at 0° C. The reaction mixture was allowed to stir for 2 hours to room temperature. The reaction mixture was washed with saturated sodium bicarbonate solution (25 ml), dried (MgSO4), filtered and evaporated. The residues were purified by column chromatography eluting with increasingly polar mixtures of methylene chloride/methanol (100/0 to 90/10), followed by methylene chloride/methanol (saturated with ammonia) (90/10). The fractions containing the desired product were combined and evaporated under vacuum to give the title product as a white foam (0.125 g, 45%); 1H NMR Spectrum: (DMSO d6) 1.50-1.65 (m, 1H); 1.65-1.80 (m, 1H); 1.95-2.15 (m, 2H); 2.25 (s, 6H); 3.10-3.50 (m, 4H); 3.75-4.05 (m, 2H); 3.95 (s, 3H); 4.90 (m, 1H); 7.30 (m, 1H); 7.35 (s, 1H); 7.40-7.60 (m, 2H); 7.85 (s, 1H); 8.40 (s, 1H); 9.65 (s, 1H); Mass Spectrum: (M+H)+ 488.

Aufarbeitung

  1. washThe reaction mixture was washed with saturated sodium bicarbonate solution (25 ml)
  2. dry with materialdried (MgSO4)
  3. filtrationfiltered
  4. customevaporated
  5. customThe residues were purified by column chromatography
  6. washeluting
  7. temperaturewith increasingly polar mixtures of methylene chloride/methanol (100/0 to 90/10)
  8. additionThe fractions containing the desired product
  9. customevaporated under vacuum

Quellen und Nachweise

ORD-Eintrag
ord-b233cf77117745328ab9a75cf3d406fb
Quelldatensatz
uspto-grants-2009_08
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US07569577B2

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