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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 344372Generated: October 30, 2026

1,4-Dioxane hydrochloride → HCID 53740475, compound

https://huagongshe.com/reaction/344372

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,4-Dioxane hydrochlorideHCID 20443148—
ReactantHCID 53886366HCID 53886366—
ProductHCID 53740475HCID 53740475—

Reaction Conditions

Temperature0 °C

Reaction Steps

N-(4-((3R)-3-tert-Butoxycarbonylaminomethylpyrrolidin-1-yl)-butyl)-1-benzyl-1 H-indole-3-carboxamide (1.35 g) was dissolved in 4N hydrochloric acid-dioxane solution (30 ml) and the mixture was stood at room temperature for 60 min. The reaction mixture was concentrated under reduced pressure. Dimethylformamide (30 ml) was added to the residue and the mixture was neutralized with triethylamine (0.74 ml). 4-Amino-5-chloro-2-methoxybenzoic acid (0.54 g) and 1-hydroxybenzotriazole (0.40 g) were added thereto, and the mixture was stirred at 0° C. for 15 min. Then, 1-ethyl-3-(3-dimethylaminopropyl)carbodiimide hydrochloride (0.56 g) was added, and the mixture was stirred at room temperature for 8 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 1.03 g of N-(4-((3R)-3-(4-amino-5-chloro-2-methoxybenzoylaminomethyl)pyrrolidin-1-yl)butyl)-l-benzyl-1 H-indole-3-carboxamide.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05864039
Source datasetuspto-grants-1999_01
ORD IDord-ad92511a25574e2c8b600959bbcbe6dd
Source noteuspto-grants-1999_01