Hydrochloric Acid → HCID 58447828, Verbindung

HRID 1036298Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 1036298
[S:1]1[CH2:6][CH2:5][N:4]([C:7]2[N:12]=[CH:11][C:10]([CH:13](C(OCC)=O)[C:14]([O:16]CC)=[O:15])=[CH:9][CH:8]=2)[CH2:3][CH2:2]1.[OH-].[Na+].Cl.C([O-])([O-])=O.[Na+].[Na+]>O1CCOCC1.O>[S:1]1[CH2:6][CH2:5][N:4]([C:7]2[N:12]=[CH:11][C:10]([CH2:13][C:14]([OH:16])=[O:15])=[CH:9][CH:8]=2)[CH2:3][CH2:2]1

Komponenten

7

Edukt 4

HCID 313Hydrochloric AcidHCID 10340Sodium CarbonateHCID 14798Sodium HydroxideHCID 58447952HCID 58447952, Verbindung

Produkt 1

HCID 58447828HCID 58447828, Verbindung

Reagenzien, Katalysatoren, Lösungsmittel 2

HCID 962WaterLösungsmittelHCID 312751,4-DioxaneLösungsmittel

Reaktionsbedingungen

Temperatur
88 °C

Versuchsvorschrift

2-(6-Thiomorpholinopyridin-3-yl)malonate 219-3 (564 mg, 1.67 mmol) was stirred with NaOH (334 mg, 8.35 mmol) in dioxane (5 ml) and water (5 ml) for 4 hours. HCl solution was added to adjust the pH around 1 and the reaction mixture heated at 88° C. for 1 hour. Then Na2CO3 was used to adjust the pH to around 4 before the solvents were evaporated. The residue was extracted with ethyl acetate and the organic extraction dried over Na2SO4 and concentrated by rotary evaporation. Purification with reverse phase HPLC afforded 2-(6-thiomorpholinopyridin-3-yl)acetic acid 219-4.

Aufarbeitung

  1. customwere evaporated
  2. extractionThe residue was extracted with ethyl acetate
  3. extractionthe organic extraction
  4. dry with materialdried over Na2SO4
  5. concentrationconcentrated by rotary evaporation
  6. customPurification with reverse phase HPLC

Quellen und Nachweise

ORD-Eintrag
ord-976bcf24e7ad4eb0be4c679650760572
Quelldatensatz
uspto-grants-2013_10
Patentnummer
US08546396B2

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