Bromopyruvic Acid → 2-(Isopropylamino)thiazole-4-carboxylic acid hydrobromide
Reaktionsgleichung
[CH:1]([NH:4][C:5]([NH2:7])=[S:6])([CH3:3])[CH3:2].[Br:8][CH2:9][C:10](=O)[C:11]([OH:13])=[O:12]>O1CCOCC1>[BrH:8].[CH:1]([NH:4][C:5]1[S:6][CH:9]=[C:10]([C:11]([OH:13])=[O:12])[N:7]=1)([CH3:3])[CH3:2]Komponenten
4
Edukt 2
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Reaktionsbedingungen
- Temperatur
- 80 °C
Versuchsvorschrift
A suspension of compound 68 (2.1 g, 18 mmol) and 3-bromopyruvic acid (3.0 g, 18 mmol) in dioxane (180 mL) was heated to 80° C. Upon reaching 80° C. the mixture became clear, and soon thereafter the product started to precipitate as a white solid. After 2 h of heating, the reaction mixture was cooled to rt and the precipitate was filtered off and collected. This yielded pure title product (4.4 g, 94%).
Aufarbeitung
- customUpon reaching 80° C.
- customto precipitate as a white solid
- temperatureAfter 2 h of heating
- temperaturethe reaction mixture was cooled to rt
- filtrationthe precipitate was filtered off
- customcollected
Quellen und Nachweise
- ORD-Eintrag
- ord-6eaf6b238aef415ea629625e8180a87d
- Quelldatensatz
- uspto-grants-2010_03
- Patentnummer
- US07671032B2
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