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1,1'-Carbonyldiimidazole → (S)-N-[5-(4-Methylpiperazin-1-yl)-3,4-dihydro-2H-1-benzopyran-3-yl]-5-methylpyridine-3-carboxamide

HRID 131132
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 131132
[CH3:1][C:2]1[CH:3]=[N:4][CH:5]=[C:6]([CH:10]=1)[C:7]([OH:9])=O.C(N1C=CN=C1)(N1C=CN=C1)=O.[NH2:23][C@H:24]1[CH2:29][C:28]2[C:30]([N:34]3[CH2:39][CH2:38][N:37]([CH3:40])[CH2:36][CH2:35]3)=[CH:31][CH:32]=[CH:33][C:27]=2[O:26][CH2:25]1>CN(C)C=O>[CH3:40][N:37]1[CH2:38][CH2:39][N:34]([C:30]2[C:28]3[CH2:29][C@H:24]([NH:23][C:7]([C:6]4[CH:5]=[N:4][CH:3]=[C:2]([CH3:1])[CH:10]=4)=[O:9])[CH2:25][O:26][C:27]=3[CH:33]=[CH:32][CH:31]=2)[CH2:35][CH2:36]1
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

5

Edukt 3

HCID 682631,1'-CarbonyldiimidazoleHCID 2562085-Methylnicotinic acidHCID 11139461(S)-3-amino-5-(4-methylpiperazin-1-yl)-1,4-dihydro-2H-1-benzopyran

Produkt 1

HCID 69207425(S)-N-[5-(4-Methylpiperazin-1-yl)-3,4-dihydro-2H-1-benzopyran-3-yl]-5-methylpyridine-3-carboxamideAusbeute 35 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 6228
Dimethylformamide
Lösungsmittel
2×

Versuchsvorschrift

A solution of 5-methylnicotinic acid (141 mg, 1.03 mmol) and 1,1′-carbonyldiimidazole (183 mg, 1.13 mmol) in anhydrous N,N-dimethylformamide (5 mL) was stirred at 75° C. for 55 min. The mixture was allowed to cool, and a solution of (S)-3-amino-5-(4-methylpiperazin-1-yl)-3,4-dihydro-2H-1-benzopyran (232 mg, 0.94 mmol) in N,N-dimethylformamide (5 mL) was added. The reaction mixture was stirred at room temperature for 28 h. The solvent was removed in vacuo, and the residue was purified by column chromatography on silica (eluent: chloroform/ethanol; 87:13+0.5% NH3). The product was contaminated with a large amount of imidazole which could be removed by the following procedure: The mixture was dissolved in diethyl ether (100 mL), washed with water (2+20 mL) and treated with brine (10 mL). The ethereal layer was dried (MgSO4), and the solvent was removed in vacuo to give 119 mg (35% yield) of the title compound as a white solid: mp sinters >68° C.; [α]21D −82° (c 1.0, chloroform); EIMS (70 eV) m/z (relative intensity) 366 (21, M+).

Aufarbeitung

  1. temperatureto cool
  2. customThe solvent was removed in vacuo
  3. customthe residue was purified by column chromatography on silica (eluent: chloroform/ethanol; 87:13+0.5% NH3)
  4. customcould be removed by the following procedure
  5. dissolutionThe mixture was dissolved in diethyl ether (100 mL)
  6. washwashed with water (2+20 mL)
  7. additiontreated with brine (10 mL)
  8. dry with materialThe ethereal layer was dried (MgSO4)
  9. customthe solvent was removed in vacuo

Quellen und Nachweise

ORD-Eintrag
ord-c3002aa0348742e5a93313e77a962113
Quelldatensatz
uspto-grants-2008_06
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US07384943B2

Notizen zur Reaktion

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