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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1926776Generated: October 25, 2026

Acetic Acid → HCID 67113605, compound

https://huagongshe.com/reaction/1926776

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
Reactant2-Aminophenylacetic acidHCID 583776—
ReactantSodium triacetoxyborohydrideHCID 5049666—
Reactant1-tosyl-1H-pyrazole-4-carbaldehydeHCID 57743031—
SolventWaterHCID 962—
SolventOxolane--water (1/1)HCID 21881883—
ProductHCID 67113605HCID 671136058%

Reaction Conditions

Temperature0 °C

Reaction Steps

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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08183241B2
Source datasetuspto-grants-2012_05
ORD IDord-2b85727c249f47879ac9f96d57484f3d
Source noteuspto-grants-2012_05