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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1896402Erstellt: 25. Oktober 2026

Acetic Acid → HCID 67113605, Verbindung

https://huagongshe.com/reaction/1896402

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktAcetic AcidHCID 176—
Edukt2-Aminophenylacetic acidHCID 583776—
EduktSodium triacetoxyborohydrideHCID 5049666—
Edukt1-tosyl-1H-pyrazole-4-carbaldehydeHCID 57743031—
LösungsmittelWaterHCID 962—
LösungsmittelOxolane--water (1/1)HCID 21881883—
ProduktHCID 67113605HCID 671136058%

Reaktionsbedingungen

Temperatur0 °C

Reaktionsschritte

In a 100 ml, three-necked flask fitted with a magnetic stirrer, 1-[(4-methylphenyl)sulfonyl]-1H-pyrazole-4-carbaldehyde x58 (1.65 g, 6.6 mmol) is dissolved in a 1/1 mixture of THF/H2O (50 ml) and the solution containing (2-aminophenyl)acetic acid x96 (1 g, 66 mmol) is added. The pH is adjusted to 5 with acetic acid and the mixture is cooled to 0° C. Sodium triacetoxyborohydride (2.10 g, 10 mmol) is added and the mixture is stirred overnight at room temperature. Water is added and the aqueous phase is extracted three times with CH2Cl2. The combined organic phases are washed with brine, dried over MgSO4 and evaporated. Purification of the residue by preparative chromatography on silicagel and recrystallization from AcOEt affords 106 mg of pure 1-(1H-pyrazol-4-ylmethyl)-1,3-dihydro-2H-indol-2-one hydrate 173.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08518943B2
Quelldatensatzuspto-grants-2013_08
ORD IDord-b78794672abf4d87ad4b87775029e55e
Quellennotizuspto-grants-2013_08