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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1851396Generated: November 2, 2026

Hydrochloric Acid → HCID 57901578, compound

https://huagongshe.com/reaction/1851396

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantEthyl 1-(methoxymethyl)-7-{methyl[(4-nitrophenyl)sulfonyl]amino}-1H-indole-2-carboxylateHCID 57901774—
SolventEthanolHCID 702—
ProductHCID 57901578HCID 5790157826%

Reaction Conditions

Temperature70 °C

Reaction Steps

To a solution of ethyl 1-(methoxymethyl)-7-{methyl[(4-nitrophenyl)sulfonyl]amino}-1H-indole-2-carboxylate (1.42 g) in ethanol (10 mL) was added 6N hydrochloric acid (10 mL), and the mixture was stirred at 70° C. for 12 hr. The reaction mixture was concentrated, water was added, and the mixture was extracted with ethyl acetate. The ethyl acetate layer was washed with saturated brine, dried (MgSO4) and concentrated. The obtained residue was dissolved in N,N-dimethylformamide (8 mL), lithium hydroxide (520 mg) and mercaptoacetic acid (430 μL) were added, and the mixture was stirred at room temperature for 12 hr. To the reaction mixture was added methyl iodide (100 μL), and the mixture was stirred at room temperature for 1 hr. Saturated aqueous sodium hydrogencarbonate solution was added to the reaction solution, and the mixture was extracted with ethyl acetate. The ethyl acetate layer was washed with saturated brine, dried (MgSO4) and concentrated. The obtained residue was subjected to silica gel column chromatography (ethyl acetate:hexane=1:1) to give a yellow amorphous (182 mg, yield 26%). M+1=219.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08957070B2
Source datasetuspto-grants-2015_02
ORD IDord-c75fe21bba54427089fd445f0f4165c9
Source noteuspto-grants-2015_02