1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimide → 5-Chloro-N-(1,3-dioxo-2-{2-oxo-2-[4-(4-pyridinyl)piperazino]ethyl}-2,3-dihydro-1H-isoindol-4-yl)-2-thiophenecarboxamide

HRID 457739Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 457739
[Cl:1][C:2]1[S:6][C:5]([C:7]([NH:9][C:10]2[CH:18]=[CH:17][CH:16]=[C:15]3[C:11]=2[C:12](=[O:24])[N:13]([CH2:20][C:21]([OH:23])=O)[C:14]3=[O:19])=[O:8])=[CH:4][CH:3]=1.O.O[N:27]1[C:31]2[CH:32]=[CH:33][CH:34]=[CH:35]C=2N=N1.CN(C)CCCN=[C:42]=[N:43][CH2:44][CH3:45].[CH:47]([N:50](C(C)C)CC)(C)C>CN(C=O)C.O>[Cl:1][C:2]1[S:6][C:5]([C:7]([NH:9][C:10]2[CH:18]=[CH:17][CH:16]=[C:15]3[C:11]=2[C:12](=[O:24])[N:13]([CH2:20][C:21](=[O:23])[N:43]2[CH2:42][CH2:47][N:50]([C:33]4[CH:32]=[CH:31][N:27]=[CH:35][CH:34]=4)[CH2:45][CH2:44]2)[C:14]3=[O:19])=[O:8])=[CH:4][CH:3]=1

Komponenten

7

Edukt 4

HCID 159081-Ethyl-3-(3'-dimethylaminopropyl)carbodiimideHCID 81531DiisopropylethylamineHCID 27960291-Hydroxybenzotriazole hydrateHCID 12074875HCID 12074875, Verbindung

Produkt 1

HCID 99579765-Chloro-N-(1,3-dioxo-2-{2-oxo-2-[4-(4-pyridinyl)piperazino]ethyl}-2,3-dihydro-1H-isoindol-4-yl)-2-thiophenecarboxamide

Reagenzien, Katalysatoren, Lösungsmittel 2

HCID 962WaterLösungsmittelHCID 6228DimethylformamideLösungsmittel

Versuchsvorschrift

0.43 g (1.18 mmol) of 2-(4-{[(5-chloro-2-thienyl)carbonyl]amino}-1,3-dioxo-1,3-dihydro-2H-isoindol-2-yl)acetic acid is dissolved in 15 ml DMF, 0.2 g (1.3 equivalents) 1-hydroxy-1H-benzotriazole hydrate (HOBT) and 0.238 g of N′-(3-dimethylaminopropyl)-N-ethylcarbodiimide (EDCI) (1.3 equivalents) are added and 0.305 g (0.411 ml; 2 equivalents) of diisopropylethylamine (DIEA) is added dropwise at room temperature over a period of 15 min. The mixture is stirred at room temperature overnight, the suspension turning into a clear solution. Water is then added to the reaction mixture, the aqueous phase is extracted three times with ethyl acetate, the combined organic phases are dried and concentrated under reduced pressure and the residue is coevaporated three times with toluene. The residue is suspended in toluene, filtered and washed with toluene. Drying gives 0.458 g (76.4% of theory) of the target compound of m.p. 207° C.

Aufarbeitung

  1. extractionthe aqueous phase is extracted three times with ethyl acetate
  2. customthe combined organic phases are dried
  3. concentrationconcentrated under reduced pressure
  4. filtrationfiltered
  5. washwashed with toluene
  6. customDrying
  7. customgives 0.458 g (76.4% of theory) of the target compound of m.p. 207° C.

Quellen und Nachweise

ORD-Eintrag
ord-150dead56a8a402d8c2390f155ab8f58
Quelldatensatz
uspto-grants-2007_03
Patentnummer
US07189738B2

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