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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1645178Generated: October 27, 2026

Hydrochloric Acid → 1-(3,5-Difluoro-benzyl)-3-(2-nitro-phenylsulfanyl)-1H-indole-6-carboxylic acid

https://huagongshe.com/reaction/1645178

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantLithium hydroxide, monohydrateHCID 168937—
Reactant1-(3,5-Difluoro-benzyl)-3-(2-nitro-phenylsulfanyl)-1H-indole-6-carboxylic acid methyl esterHCID 59463826—
SolventWaterHCID 962—
Solvent1,4-DioxaneHCID 31275—
Product1-(3,5-Difluoro-benzyl)-3-(2-nitro-phenylsulfanyl)-1H-indole-6-carboxylic acidHCID 5946385089%

Reaction Conditions

Temperature60 °C

Reaction Steps

To a solution of 1-(3,5-Difluoro-benzyl)-3-(2-nitro-phenylsulfanyl)-1H-indole-6-carboxylic acid methyl ester (150.0 mg, 0.33 mmol) in dioxane (20 mL) and water (15 mL) was added LiOH.H2O (83.1 mg, 2.0 mmol) in 5 ml water. The reaction mixture was stirred overnight at 60° C. The mixture was then acidified to pH 4 by addition of 15% aqueous HCl and the mixture was extracted twice with ethyl acetate. The combined organic layers were dried over Na2SO4 and concentrated in vacuo to give a yellow powder. The product was recrystallised from heptane/ethyl acetate to give the title compound as yellow/orange crystals (129.3 mg, y=89%)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08124647B2
Source datasetuspto-grants-2012_02
ORD IDord-e94bc8cbf58e495286380af33bd7ac32
Source noteuspto-grants-2012_02