Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 344371Generated: October 31, 2026

1,4-Dioxane hydrochloride → HCID 54557691, compound

https://huagongshe.com/reaction/344371

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,4-Dioxane hydrochlorideHCID 20443148—
ReactantHCID 54300511HCID 54300511—
ProductHCID 54557691HCID 54557691—

Reaction Steps

N-(4-((3R)-3-tert-Butoxycarbonylaminomethylpyrrolidin-1-yl)-butyl)-1-isopropyl-1 H-indole-3-carboxamide (1.34 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 (0.81 ml). 4-Amino-5-chloro-2-methoxybenzoic acid (0.59 g) and 1-hydroxybenzotriazole (0.44 g) were added thereto, and the mixture was stirred at 0C for 15 min. Then, 1-ethyl-3-(3-dimethylaminopropyl)carbodiimide hydrochloride (0.62 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 0.62 g of N-(4-((3R)-3-(4-amino-5-chloro-2-methoxybenzoylaminomethyl)pyrrolidin-1-yl)butyl)-1-isopropyl-1 H-indole-3-carboxamide.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05864039
Source datasetuspto-grants-1999_01
ORD IDord-5863c3d2457c46b8b8f9d9fabbe4a78e
Source noteuspto-grants-1999_01