HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → 6-bromo-3-iodo-N-(4-methoxybenzyl)quinolin-2-amine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | 4-Methoxybenzylamine | HCID 75452 | — |
| Reactant | 6-Bromo-2-chloro-3-iodoquinoline | HCID 86676837 | — |
| Solvent | N-methyl-2-pyrrolidone | HCID 13387 | — |
| Product | 6-bromo-3-iodo-N-(4-methoxybenzyl)quinolin-2-amine | HCID 67345652 | — |
Reaction Conditions
| Temperature | 130 °C |
|---|
Reaction Steps
A glass microwave reaction vessel was charged with 6-bromo-2-chloro-3-iodoquinoline (0.918 g, 2.492 mmol) and 4-methoxybenzylamine (2.279 mL, 17.44 mmol) in N-methyl-2-pyrrolidinone (3.56 mL). The reaction mixture was stirred and heated in a microwave reactor at 130° C. for 20 min. The solution was poured into water and extracted with diethyl ether. The combined organic extracts were washed with saturated ammonium chloride, water, saturated sodium chloride, and dried over magnesium sulfate. The solution was filtered and concentrated in vacuo to give the crude material 6-bromo-3-iodo-N-(4-methoxybenzyl)quinolin-2-amine as a tan solid which was used without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08735384B2 |
| Source dataset | uspto-grants-2014_05 |
| ORD ID | ord-52f3dfeb604f4fb4ad89172184062663 |
| Source note | uspto-grants-2014_05 |