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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1067828Generated: October 30, 2026

Guanidine Hydrochloride → HCID 178485148, compound

https://huagongshe.com/reaction/1067828

Reaction equation

Participants

RoleNameHCIDCharge
ReactantGuanidine HydrochlorideHCID 5742—
ReactantSodium MethoxideHCID 10942334—
ReactantEthyl 4-chloro-1-methyl-6-(2-nitrophenoxy)-2-indolecarboxylateHCID 21194137—
SolventMethanolHCID 887—
ProductHCID 178485148HCID 17848514840.1%

Reaction Steps

After 2.87 g (30.0 mmol) of guanidine hydrochloride was added to 25 ml of a methanol solution of 1.62 g (30.0 mmol) of sodium methoxide, the mixture was stirred at room temperature for 30 minutes. The precipitated sodium chloride was filtered off. To the obtained solution was added 0.51 g (1.50 mmol) of ethyl 4-chloro-1-methyl-6-(2-nitrophenoxy)-2-indolecarboxylate. Subsequently methanol was distilled off under reduced pressure. The resulting residue was heated at 130° C. for 5 minutes and then allowed to stand at room temperature for an hour. Thereafter water was poured onto the reaction solution and the mixture was extracted three times with ethyl acetate. The combined extracts were washed with water. After drying over anhydrous magnesium sulfate, the solvent was distilled off under reduced pressure. The resulting residue was isolated and purified by silica gel column chromatography to give 0.23 g (40.1%) of 4-chloro-1-methyl-6-(2-nitrophenoxy)-2-indoloylguanidine.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06248772B1
Source datasetuspto-grants-2001_06
ORD IDord-13ccadf78e7c46eb8a96190fdd7dca03
Source noteuspto-grants-2001_06