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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1645337Generated: October 30, 2026

4-{4-[(4,5-dichloro-1-ethyl-1H-indole-2-carbonyl)-amino]-phenyl}-piperazine-1-carboxylic acid tert-butyl ester → 4,5-Dichloro-1-ethyl-1h-indole-2-carboxylic acid (4-piperazin-1-yl-phenyl)-amide hydrochloride salt

https://huagongshe.com/reaction/1645337

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-{4-[(4,5-dichloro-1-ethyl-1H-indole-2-carbonyl)-amino]-phenyl}-piperazine-1-carboxylic acid tert-butyl esterHCID 59365131—
SolventHydrochloric AcidHCID 313—
SolventDichloromethaneHCID 6344—
Solvent1,4-DioxaneHCID 31275—
Product4,5-Dichloro-1-ethyl-1h-indole-2-carboxylic acid (4-piperazin-1-yl-phenyl)-amide hydrochloride saltHCID 66772391212.8%

Reaction Steps

A mixture of 4-{4-[(4,5-dichloro-1-ethyl-1H-indole-2-carbonyl)-amino]-phenyl}-piperazine-1-carboxylic acid tert-butyl ester (750 mg, 1.45 mmol) in 15 mL of methylene chloride and 2 mL of 4M hydrogen chloride in dioxane was stirred at room temperature for 24 hr. The solvent was removed to afford 4,5-dichloro-1-ethyl-1H-indole-2-carboxylic acid (4-piperazin-1-yl-phenyl)-amide hydrochloride salt (700 mg, 99% yield) as an off white solid. LCMS for C21H22Cl2N4O calcd. (m/e) 416, observed 417 (M+H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08124766B2
Source datasetuspto-grants-2012_02
ORD IDord-7f2ea9fa88c944269e0624e855b213dc
Source noteuspto-grants-2012_02