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

Hydrochloric Acid → HCID 178468723, Verbindung

HRID 258560
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 258560
C1(CCC(C(C(OCC)=O)C(OCC)=O)=O)C=CC=CC=1.NC1N(CC)N=CC=1.Cl.Cl.[CH2:32]([N:34]1[C:38]2=[N:39][C:40]([CH2:49][CH2:50][C:51]3[CH:56]=[CH:55][CH:54]=[CH:53][CH:52]=3)=[C:41]([C:44]([O:46][CH2:47][CH3:48])=[O:45])[C:42]([OH:43])=[C:37]2[CH:36]=[N:35]1)[CH3:33]>C(O)C.C(OCC)(=O)C.CCOCC.O>[CH2:32]([N:34]1[C:38]2=[N:39][C:40]([CH2:49][CH2:50][C:51]3[CH:52]=[CH:53][CH:54]=[CH:55][CH:56]=3)=[C:41]([C:44]([O:46][CH2:47][CH3:48])=[O:45])[C:42]([OH:43])=[C:37]2[CH:36]=[N:35]1)[CH3:33]
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

8

Edukt 4

HCID 313Hydrochloric AcidHCID 3373101-Ethyl-1H-pyrazol-5-amineHCID 10989977Propanedioic acid, (1-oxo-3-phenylpropyl)-, diethyl esterHCID 178468724HCID 178468724, Verbindung

Produkt 1

HCID 178468723HCID 178468723, Verbindung

Reagenzien, Katalysatoren, Lösungsmittel 3

HCID 962
Water
Lösungsmittel
HCID 3283Diethyl EtherLösungsmittel
HCID 21584252Ethanol ethylacetateLösungsmittel

Versuchsvorschrift

43.6 g. of (3-phenylpropionyl)malonic acid, diethyl ester (0.15 mol.) are added to a stirred mixture of 16.5 g. of 5-amino-1-ethylpyrazole (0.15 mol.) and 220 g. of polyphosphoric acid. The mixture is heated to 120° (bath temperature) for 50 minutes. After the mixture has cooled to room temperature, 250 ml. of water are added in portions and stirring is continued for 20 minutes. The aqueous phosphoric acid solution is then decanted and the undissolved residue is treated with 200 ml. of water and aqueous ammonia (10%) to neutralize the mixture. The mixture is extracted with chloroform and the chloroform extract is washed twice with water, dried with Na2SO4 and evaporated to yield 39 g. of the oily product. Dissolution of the oil in about 250 ml. of ether and addition of ethereal hydrogen chloride yields 35 g. (62%) of 1-ethyl-4-hydroxy-6-(2-phenylethyl)-1H-pyrazolo[3,4-b]pyridine-5-carboxylic acid, ethyl ester, hydrochloride, m.p. 153°-155° (ethanol/ethyl acetate 1:1).

Aufarbeitung

  1. temperatureThe mixture is heated to 120° (bath temperature) for 50 minutes
  2. customThe aqueous phosphoric acid solution is then decanted
  3. additionthe undissolved residue is treated with 200 ml
  4. extractionThe mixture is extracted with chloroform
  5. extractionthe chloroform extract
  6. washis washed twice with water
  7. dry with materialdried with Na2SO4
  8. customevaporated
  9. customto yield 39 g
  10. dissolutionDissolution of the oil in about 250 ml
  11. customyields 35 g

Quellen und Nachweise

ORD-Eintrag
ord-757c504b9c504e5e93baa0f42c8ef911
Quelldatensatz
uspto-grants-1977_07
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US04033970

Notizen zur Reaktion

Wird geladen…

Auf dieser SeiteKomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion