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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2260114Generated: November 4, 2026

Water → HCID 18999800, compound

https://huagongshe.com/reaction/2260114

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantAcetic AnhydrideHCID 7918—
ReactantSodium hydrideHCID 24758—
ReactantHCID 9860908HCID 9860908—
SolventTetrahydrofuranHCID 8028—
ProductHCID 18999800HCID 18999800—
ProductHCID 69840660HCID 69840660—

Reaction Steps

To an ice-colded suspension of NaH (0.029 g) in 30 ml of anhydrous THF under N2 is added 7-(3-fluoro-4-methoxyphenyl)-1H-pyrazolo[3,4-g]quinoxaline (0.30 g). The orange-red mixture is stirred at the same temperature for 5 minutes, then acetic anhydride (0.122 g) is added dropwise to the mixture. A yellow solid forms during the acetic anhydride additions. The resulting mixture is stirred at room temperature overnight. The mixture is poured into water. The yellow solid is filtered, washed with water then with ether and dried. The product is purified by column chromatography eluting with 15% ethylacetate in hexane, 25% ethylacetate in hexane then 5% ethylacetate in methylene chloride to obtain 1-acetyl-7-(3-fluoro-4-methoxyphenyl)-1H-pyrazolo[3,4-g]quinoxaline (m.p. 261°-265° C.) and 1-acetyl-7-(3-fluoro-4-methoxyphenyl)-2H-pyrazolo[3,4-g]quinoxaline.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05476851
Source datasetuspto-grants-1995_12
ORD IDord-b0076ce25ed6485da41c3f8995907882
Source noteuspto-grants-1995_12