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

Water → (2S)-2-[[4-[(2-amino-5-formyl-4-oxo-1,6,7,8-tetrahydropteridin-6-yl)methylamino]benzoyl]amino]pentanedioic acid

HRID 615686
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 615686
[C:1]([OH:33])(=[O:32])[CH2:2][CH2:3][C@H:4]([NH:8][C:9]([C:11]1[CH:31]=[CH:30][C:14]([N:15]2[CH2:27][CH:26]3[N+:17]([C:18]4[C:19](=[O:29])[NH:20][C:21]([NH2:28])=[N:22][C:23]=4[NH:24][CH2:25]3)=[CH:16]2)=[CH:13][CH:12]=1)=[O:10])[C:5]([OH:7])=[O:6].[OH2:34]>>[CH:12]1[C:11]([C:9]([NH:8][C@H:4]([C:5]([OH:7])=[O:6])[CH2:3][CH2:2][C:1]([OH:33])=[O:32])=[O:10])=[CH:31][CH:30]=[C:14]([NH:15][CH2:27][CH:26]2[N:17]([CH:16]=[O:34])[C:18]3[C:19]([N:20]=[C:21]([NH2:28])[NH:22][C:23]=3[NH:24][CH2:25]2)=[O:29])[CH:13]=1
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

3

Edukt 2

HCID 962WaterHCID 1353986575,10-Methenyltetrahydrofolate

Produkt 1

HCID 178508910(2S)-2-[[4-[(2-amino-5-formyl-4-oxo-1,6,7,8-tetrahydropteridin-6-yl)methylamino]benzoyl]amino]pentanedioic acid

Versuchsvorschrift

The reaction of this invention comprises mixing 5,10-methenyl-5,6,7,8-tetrahydrofolic acid (anhydroleucovorin), an amine base, and water and heating the mixture at a temperature of from about 50° C. to reflux for a period of time of from about 30 min to about 10 hours, perferably about 4-6 hours, at a pH of from about 5-7 to give leucovorin. The pH of the mixture is adjusted to and maintained at 5 to 7 by the addition or removal, as appropriate, of suitable amounts of the amine bases useful in this invention. The anhydroleucovorin may be used in the form of its internal salt (i.e. zwitterion) or as a salt with a suitable anion, preferably chloride, normally as a hydrate. After the ring opening reaction is complete, the reaction mixture is generally cooled and filtered. Slightly more than an equimolar (to anhydroleucovorin) amount of a water soluble calcium salt, e.g. chloride, bromide, iodide, nitrate, acetate, is then added either as an aqueous solution or as a solid to the filtrate and calcium leucovorin is precipitated by adding a water soluble organic solvent, e.g. a lower alkanol such as methanol, ethanol, isopropanol, or acetone. The calcium leucovorin is than removed by filtration, washed with a suitable solvent such as aqueous ethanol, ethanol, acetone, ether, ethyl acetate or the like and dried. Column chromatography is generally not required since the product so obtained meets or exceeds USP specifications.

Aufarbeitung

  1. customThe reaction of this invention
  2. temperatureto reflux for a period of time of from about 30 min to about 10 hours, perferably about 4-6 hours, at a pH of from about 5-7

Quellen und Nachweise

ORD-Eintrag
ord-7b04471d23a64095bb3651ea0c994de5
Quelldatensatz
uspto-grants-1985_02
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US04500711

Notizen zur Reaktion

Wird geladen…

Auf dieser SeiteKomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion