HuagongsheHuagongshe Chemistry Print Report · For research reference only
N-Methylbenzylamine → 2-Aminoquinoline
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | N-Methylbenzylamine | HCID 7669 | — |
| Reactant | 6-Bromo-2-chloroquinoline | HCID 12894086 | — |
| Product | 2-Aminoquinoline | HCID 11379 | — |
Reaction Steps
6-Bromo-2-chloroquinoline (200 mg, 0.8 mmol) and N-methylbenzylamine (2 mL) were heated at 120° C. for 16 hours. Extraction from 2M NaOH into DCM and drying on Na2SO4 gave the crude 2-aminoquinoline. This was converted, via Methods 3 and 5, to compound 204 (110 mg, 46%). [M−H]−=291.1 m/z. Activity: A
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08957049B2 |
| Source dataset | uspto-grants-2015_02 |
| ORD ID | ord-377296de01c34f1b8da6ec767d37f6ac |
| Source note | uspto-grants-2015_02 |