StartseiteMCPWorkbenchSkills
StartseiteWorkbenchBenachrichtigungenMein Bereich
llms.txt · MCP-AnleitungDatenschutz · Nutzungsbedingungen · Supportv1.8.0
  1. Startseite
  2. /Reaktion

Hydrochloric Acid → Octahydropyrazino[2,1-c][1,4]thiazine 2,2-dioxide

HRID 2074835
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 2074835
[CH2:1]1[CH:6]2[C:7](=O)[NH:8][CH2:9][CH2:10][N:5]2[CH2:4][CH2:3][S:2]1(=[O:13])=[O:12].Cl>C1COCC1>[CH2:1]1[CH:6]2[CH2:7][NH:8][CH2:9][CH2:10][N:5]2[CH2:4][CH2:3][S:2]1(=[O:13])=[O:12]
KomponentenReaktionsbedingungenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

4

Edukt 2

HCID 313Hydrochloric AcidHCID 59215885Hexahydropyrazino[2,1-c][1,4]thiazin-9(6H)-one 2,2-dioxide

Produkt 1

HCID 59215787Octahydropyrazino[2,1-c][1,4]thiazine 2,2-dioxideAusbeute 111,6 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 8028TetrahydrofuranLösungsmittel2×

Reaktionsbedingungen

Temperatur
50 °C

Versuchsvorschrift

To a suspension of hexahydropyrazino[2,1-c][1,4]thiazin-9(6H)-one 2,2-dioxide (D18; 165 mg, 0.81 mmol) in 1 ml of anhydrous THF were added successive aliquots of a 1M solution of borane THF complex in THF (total 20.4 ml, 20.4 mmol) and the reaction stirred at room temperature and 50° C., until disappearance of the starting material. Hydrochloric acid (5M, 2 ml) was added to the solution and stirring was continued at 50° C. for 12 h. The solvent was removed under reduced pressure and the residue loaded on a SCX cartridge, washed with methanol and eluted with 0.5M methanolic ammonia. The basic fractions were collected and the solvent removed leaving 172 mg of the target product, partially contaminated by the starting material.

Aufarbeitung

  1. stirringstirring
  2. customThe solvent was removed under reduced pressure
  3. washwashed with methanol
  4. washeluted with 0.5M methanolic ammonia
  5. customThe basic fractions were collected
  6. customthe solvent removed

Quellen und Nachweise

ORD-Eintrag
ord-34cfe6bec5144f36be3e34c319e9f856
Quelldatensatz
uspto-grants-2011_04
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US07919491B2

Notizen zur Reaktion

Wird geladen…

Auf dieser SeiteKomponentenReaktionsbedingungenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion