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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 502143Generated: October 31, 2026

Carbon Dioxide → HCID 11492556, compound

https://huagongshe.com/reaction/502143

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCarbon DioxideHCID 280—
Reactant2,5-DimethoxytetrahydrofuranHCID 79098—
ReactantSodium BicarbonateHCID 516892—
Reactant2-Amino-6-nitro-1H-indole-3-carbonitrileHCID 16361367—
SolventAcetic AcidHCID 176—
SolventWaterHCID 962—
ProductHCID 11492556HCID 11492556—
Product1-ethyl-6-methoxy-1H-indole-3-carbonitrileHCID 11644100—

Reaction Steps

A solution of 2-amino-6-nitro-1H-indole-3-carbonitrile (362 mg, 1.79 mmol) in acetic acid (5 mL) is treated with 2,5-dimethoxytetrahydrofuran (0.30 mL, 2.27 mmol), and the solution is heated to reflux for 14 h. After cooling to ambient temperature, the solution is poured into water (100 mL), and solid sodium bicarbonate is added until CO2 evolution ceased. The mixture is extracted with EtOAc (2×100 mL), and the extracts are washed with saturated brine, combined, dried over MgSO4, filtered and concentrated. The residual material is separated by silica gel chromatography (EtOAc/hexanes, 1/4) to afford 6-nitro-2-pyrrol-1-yl-1H-indole-3-carbonitrile, compound 5, as a yellow solid (232 mg, 51%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07772271B2
Source datasetuspto-grants-2010_08
ORD IDord-50484a7123a546c18af1667e89f08c46
Source noteuspto-grants-2010_08