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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 344367Generated: October 29, 2026

HCID 15866639, compound → HCID 9915250, compound

https://huagongshe.com/reaction/344367

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 15866639HCID 15866639—
Reactant1,4-Dioxane hydrochlorideHCID 20443148—
ProductHCID 9915250HCID 9915250—

Reaction Conditions

Temperature0 °C

Reaction Steps

N-(5-(4-tert-Butoxycarbonylaminomethylpiperidin-1-yl)pentyl)-1-methyl-1 H-indole-3-carboxamide (1.12 g) was dissolved in 4N hydrochloric acid-dioxane solution (30 ml) and the mixture was stood at room temperature for 1 hr. The reaction mixture was concentrated under reduced pressure. Dimethylformamide (30 ml) was added to the residue and the mixture was neutralized with triethylamine (0.68 ml). 4-Amino-5-chloro-2-methoxybenzoic acid (0.49 g) and 1-hydroxybenzotriazole (0.36 g) were added thereto, and the mixture was stirred at 0° C. for 20 min. Then, 1-ethyl-3-(3-dimethylaminopropyl)carbodiimide hydrochloride (0.52 g) was added, and the mixture was stirred at room temperature for 12 hr. The reaction mixture was concentrated under reduced pressure. Aqueous potassium carbonate solution was added to the residue and the mixture was extracted with ethyl acetate. The extract was dried over magnesium sulfate and concentrated under reduced pressure. The obtained residue was purified by silica gel chromatography to give 0.60 g of N-(5-(4 -(4-amino-5-chloro-2-methoxybenzoylaminomethyl)piperidin-1-yl)pentyl)-l-methyl-1 H-indole-3-carboxamide.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05864039
Source datasetuspto-grants-1999_01
ORD IDord-46d670fbf04b4c59a685373333eaf0e9
Source noteuspto-grants-1999_01