HuagongsheHuagongshe Chemistry Print Report · For research reference only
Pyridine → HCID 22641330, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Pyridine | HCID 1049 | — |
| Reactant | Sodium Iodide | HCID 5238 | — |
| Reactant | Pyrrolidine | HCID 31268 | — |
| Reactant | HCID 22641470 | HCID 22641470 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 22641330 | HCID 22641330 | 68.2% |
Reaction Steps
A suspension of 1 g (3.5 mmol) of 6-bromo-4-chloro-7-methoxy-2-methyl-quinoline in 20 ml of EtOH was treated sequentially at RT and under stirring with 0.49 g (7 mmol) of pyrrolidine, 0.137 g (1.4 mmol) of pyridine and a catalytic amount of NaI. The mixture was then heated to reflux for 20 h, cooled to RT and concentrated in vacuo. The residue was applied to a silica gel column with CH2Cl2/MeOH (7:1) as eluent. Combinations of the purified fractions and concentration in vacuo gave 0.85 g (68.2%) of the 6-bromo-7-methoxy-2-methyl-4-pyrrolidin-1-yl-quinoline hydrochloride as light brown solid. ISP mass spectrum, m/e: 323.3 (M+1 calculated for C15H17BrN2O: 323).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06818767B2 |
| Source dataset | uspto-grants-2004_11 |
| ORD ID | ord-392b3aeca1a844c5a1a359c33937df6d |
| Source note | uspto-grants-2004_11 |