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Ammonium Hydroxide → 4-Cyano-3-iodo-5-(methylsulfanyl)thiophene-2-carboxamide

HRID 2091683
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 2091683
[C:1]([C:3]1[C:4]([I:13])=[C:5]([C:10](O)=[O:11])[S:6][C:7]=1[S:8][CH3:9])#[N:2].Cl.C[N:16](C)CCCN=C=NCC.ON1C2C=CC=CC=2N=N1.[OH-].[NH4+]>C(Cl)Cl.CO.O>[C:1]([C:3]1[C:4]([I:13])=[C:5]([C:10]([NH2:16])=[O:11])[S:6][C:7]=1[S:8][CH3:9])#[N:2]
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

8

Edukt 4

HCID 14923Ammonium HydroxideHCID 757711-HydroxybenzotriazoleHCID 27239391,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 580228624-Cyano-3-iodo-5-(methylsulfanyl)thiophene-2-carboxylic acid

Produkt 1

HCID 580228964-Cyano-3-iodo-5-(methylsulfanyl)thiophene-2-carboxamide

Reagenzien, Katalysatoren, Lösungsmittel 3

HCID 887MethanolLösungsmittelHCID 962WaterLösungsmittelHCID 6344DichloromethaneLösungsmittel2×

Versuchsvorschrift

To a suspension of 4-cyano-3-iodo-5-(methylsulfanyl)thiophene-2-carboxylic acid (2.85 g, 7.93 mmol) in methylene chloride (30 mL), were added N-(3-dimethylaminopropyl)-N′-ethylcarbodiimide hydrochloride (3.28 g, 17.1 mmol) and 1-hydroxybenzotriazole (2.27 g, 16.8 mmol). The reaction mixture was stirred at room temperature for two hours and ammonium hydroxide (15.4 mL) was added and the biphasic mixture was stirred at room temperature for two hours. Water (100 mL), methanol (50 mL), methylene chloride (200 mL) was added. The organic layer was removed. The aqueous layer was extracted five times with a solution of 20% methanol in methylene chloride (100 mL). The combined organic extracts were dried over anhydrous magnesium sulfate, filtered and concentrated to the title compound as dark red oil (1.47 g, 57%). LCMS: (FA) ES+ 325.

Aufarbeitung

  1. stirringthe biphasic mixture was stirred at room temperature for two hours
  2. customThe organic layer was removed
  3. extractionThe aqueous layer was extracted five times with a solution of 20% methanol in methylene chloride (100 mL)
  4. dry with materialThe combined organic extracts were dried over anhydrous magnesium sulfate
  5. filtrationfiltered
  6. concentrationconcentrated to the title compound as dark red oil (1.47 g, 57%)

Quellen und Nachweise

ORD-Eintrag
ord-a2a59f775e0843cf96eb6befe588ba8a
Quelldatensatz
uspto-grants-2013_05
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US08440664B2

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