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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 907124Generated: October 28, 2026

Carbon Dioxide → HCID 11492556, compound

https://huagongshe.com/reaction/907124

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) was treated with 2,5-dimethoxytetrahydrofuran (0.30 mL, 2.27 mmol), and the solution was heated to reflux for 14 h. After cooling to ambient temperature, the solution was poured into water (100 mL), and solid sodium bicarbonate was added until CO2 evolution ceased. The mixture was extracted with EtOAc (2×100 mL), and the extracts were washed with saturated brine, combined, dried over MgSO4, filtered and concentrated. The residual material was 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 numberUS08013006B2
Source datasetuspto-grants-2011_09
ORD IDord-88c94c076d1547f698634e383071db4a
Source noteuspto-grants-2011_09