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Hydrochloric Acid → Imidazo[1,2-a]pyridine-2-carboxylic acid

HRID 872846
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 872846
[N:1]1[C:2]([C:10]([O:12]CC)=[O:11])=[CH:3][N:4]2[CH:9]=[CH:8][CH:7]=[CH:6][C:5]=12.[OH-].[Li+].Cl>C1COCC1.O>[N:1]1[C:2]([C:10]([OH:12])=[O:11])=[CH:3][N:4]2[CH:9]=[CH:8][CH:7]=[CH:6][C:5]=12
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

6

Edukt 3

HCID 313Hydrochloric AcidHCID 3939Lithium HydroxideHCID 818807Ethyl imidazo[1,2-a]pyridine-2-carboxylate

Produkt 1

HCID 2062168Imidazo[1,2-a]pyridine-2-carboxylic acid

Reagenzien, Katalysatoren, Lösungsmittel 2

HCID 962WaterLösungsmittelHCID 8028Tetrahydrofuran
Lösungsmittel
2×

Versuchsvorschrift

Into a flask containing a mixture of ethyl imidazo[1,2-a]pyridine-2-carboxylate (1 g, 5.26 mmol), THF (5 ml) and water (5 ml), lithium hydroxide (0.378 g, 15.77 mmol) was added and stirred overnight at RT. The pH of the reaction mixture was adjusted to 2 with 2 M HCl and THF was evaporated. The remaining water phase was extracted with ethyl acetate and the combined ethyl acetate phases were dried. The product had precipitated into the water phase. Water was evaporated, and the remaining solid recrystallized from methanol. The product was used as a salt in the next step. 1H-NMR (400 MHz; DMSO-d6): δ 7.23-7.26 (m, 1H), 7.63-7.70 (m, 1H), 7.76 (dd, 1H), 8.72 (s, 1H), 8.73-8.77 (m, 1H).

Aufarbeitung

  1. additionInto a flask containing
  2. additionwas added
  3. customwas evaporated
  4. extractionThe remaining water phase was extracted with ethyl acetate
  5. dry with materialthe combined ethyl acetate phases were dried
  6. customThe product had precipitated into the water phase
  7. customWater was evaporated
  8. customthe remaining solid recrystallized from methanol

Quellen und Nachweise

ORD-Eintrag
ord-f064cd527bf84b528e6f3efe4ef403c7
Quelldatensatz
uspto-grants-2015_03
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US08975254B2

Notizen zur Reaktion

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