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

Methyl 3-oxo-3,4-dihydro-2H-1,4-benzothiazine-6-carboxylate → methyl 3,4-dihydro-2H-1,4-benzothiazine-6-carboxylate

HRID 641325
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 641325
[CH3:1][O:2][C:3]([C:5]1[CH:6]=[CH:7][C:8]2[S:13][CH2:12][C:11](=O)[NH:10][C:9]=2[CH:15]=1)=[O:4]>O1CCCC1>[CH3:1][O:2][C:3]([C:5]1[CH:6]=[CH:7][C:8]2[S:13][CH2:12][CH2:11][NH:10][C:9]=2[CH:15]=1)=[O:4]
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

3

Edukt 1

HCID 699501Methyl 3-oxo-3,4-dihydro-2H-1,4-benzothiazine-6-carboxylate

Produkt 1

HCID 17796647methyl 3,4-dihydro-2H-1,4-benzothiazine-6-carboxylateAusbeute 96 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 8028TetrahydrofuranLösungsmittel2×

Versuchsvorschrift

Borane-tetrahydrofuran complex solution (1 M in tetrahydrofuran, 45 mL, 45 mmol) was added at 0° C. to a suspension of methyl-3-oxo-3,4-dihydro-2H-1,4-benzothiazine-6-carboxylate (2.00 g, 8.96 mmol) in tetrahydrofuran (20 mL). The ice bath was removed, the homogenous solution stirred at room temperature for 2 h, then excess reagent was destroyed by careful addition of methanol (42 mL) at 0° C. After evaporation of volatile material, the residue was taken up in 5% methanolic sulfuric acid solution (25 mL) and the solution was heated at reflux over 80 min. After cooling, the reaction mixture was partitioned between ethyl acetate and water, the organic layer was dried (MgSO4) and evaporated to produce 3,4-dihydro-2H-benzo[1,4]thiazine-6-carboxylic acid methyl ester (1.79 g, 96%). Light yellow solid, MS (ISP)=210.1 (M+H)+.

Aufarbeitung

  1. customThe ice bath was removed
  2. customexcess reagent was destroyed by careful addition of methanol (42 mL) at 0° C
  3. customAfter evaporation of volatile material
  4. temperaturethe solution was heated
  5. temperatureat reflux over 80 min
  6. temperatureAfter cooling
  7. customthe reaction mixture was partitioned between ethyl acetate and water
  8. dry with materialthe organic layer was dried (MgSO4)
  9. customevaporated

Quellen und Nachweise

ORD-Eintrag
ord-174708bb10dc4ea984c2b8663f64ef1a
Quelldatensatz
uspto-grants-2010_04
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US07696200B2

Notizen zur Reaktion

Wird geladen…

Auf dieser SeiteKomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion