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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1011421Generated: October 29, 2026

Hydrochloric Acid → 1,3-Dihydro-3-(1(3H)-isobenzofuranylidene)-2H-pyrrolo[3,2-b]pyridin-2-one

https://huagongshe.com/reaction/1011421

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantPhthalideHCID 6885—
Reactant1,3-Dihydro-2H-pyrrolo[3,2-b]pyridin-2-oneHCID 316367—
ReactantSodium BicarbonateHCID 516892—
ReactantLiHMDS tetrahydrofuranHCID 23714775—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
Product1,3-Dihydro-3-(1(3H)-isobenzofuranylidene)-2H-pyrrolo[3,2-b]pyridin-2-oneHCID 6731438616%

Reaction Steps

To a solution of 1,3-dihydro-pyrrolo[3,2-b]pyridin-2-one(50 mg, 0.37 mmol) in anhydrous N,N-dimethylformamide(5.0 ml) was added 1.0M LiHMDS/THF solution (0.74 ml, 0.74 mmol) under N2. After the mixture was stirred at room temperature for 10 minutes, phthalide was added (40 mg, 0.30 mmol), and then it was continuously stirred at room temperature for 4 hours. The mixture was poured into 2M HCl (4.0 ml), heated at 50° C. for 20 minutes and then poured into water (100 ml). After cooled to room temperature, the mixture was basified to pH 9 with saturated NaHCO3 solution, and was stirred at room temperature overnight. The resulting solid was filtered, washed with water, dried under vacuum and triturated with chloroform to give 3-(3H-isobenzofuran-1-ylidene)-1,3-dihydro-pyrrolo[3,2-b]pyridin-2-one as a yellow solid (12 mg, 16%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07977351B2
Source datasetuspto-grants-2011_07
ORD IDord-91a6c5145f8f4a70a1a24da6079a0131
Source noteuspto-grants-2011_07