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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2415478Generated: October 31, 2026

Pyrrolidine → HCID 22641362, compound

https://huagongshe.com/reaction/2415478

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyrrolidineHCID 31268—
ReactantHCID 22641405HCID 22641405—
ProductHCID 22641362HCID 22641362101.2%

Reaction Steps

A solution of 1 g (3.07 mmol) of 7-benzyloxy-6-butyl-4-chloro-quinoline hydrochloride in 2.5 ml (30.7 mmol) of pyrrolidine was heated at 60° C. with stirring under an argon atmosphere for 24 h after which time the reaction was completed according to HPLC analysis. The excess pyrrolidine was evaporated off, and the residue was partitioned between EtOAc and water. The layers were separated and the aqueous layer once extracted with AcOEt. The combined organic layers were washed with water then saturated NaCl solution, dried over magnesium sulphate and concentrated in vacuo to give 1.12 g (97.4%) of the 7-benzyloxy-6-butyl-4-pyrrolidin-1-yl-quinoline as a brown oil. ISP mass spectrum, m/e: 361.3 (M+1 calculated for C24H28N2O: 361).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06818767B2
Source datasetuspto-grants-2004_11
ORD IDord-2e058e63c88e485cb2de87c08f12ee83
Source noteuspto-grants-2004_11