HuagongsheHuagongshe Chemistry Print Report · For research reference only
Pyrrolidine → HCID 22641362, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Pyrrolidine | HCID 31268 | — |
| Reactant | HCID 22641405 | HCID 22641405 | — |
| Product | HCID 22641362 | HCID 22641362 | 101.2% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06818767B2 |
| Source dataset | uspto-grants-2004_11 |
| ORD ID | ord-2e058e63c88e485cb2de87c08f12ee83 |
| Source note | uspto-grants-2004_11 |