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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 240305Generated: October 25, 2026

Methanol → 9-hydroxy-3-methoxy-9H-indeno[1,2-b]pyrazine-2-carbonitrile

https://huagongshe.com/reaction/240305

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantWaterHCID 962—
Reactant9-oxo-9H-indeno(1,2-b)pyrazine-2,3-dicarbonitrileHCID 292929—
ReactantSodium borohydrideHCID 4311764—
Product9-hydroxy-3-methoxy-9H-indeno[1,2-b]pyrazine-2-carbonitrileHCID 1606535253%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a suspension of 1 (150 mg, 0.646 mmol) in MeOH (6.5 ml), cooled at 0° C., NaBH4 (24 mg, 0.646 mmol) was added. After 30 min, water (5 ml) was added, MeOH was evaporated and the residue was extracted with CH2Cl2 (3×5 ml). The organic layers were dried over Na2SO4, filtered and evaporated. EtOH was added and the precipitate was collected by filtration affording 2 (82 mg, 53%) as white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08648076B2
Source datasetuspto-grants-2014_02
ORD IDord-53bbcc47733a4da5a71f65262cc9e700
Source noteuspto-grants-2014_02