HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Amino-4-methylpyridine → 2-(3,4-Dimethoxyphenyl)-7-methylimidazo(1,2-A)pyridine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Amino-4-methylpyridine | HCID 1533 | — |
| Reactant | 2-Bromo-1-(3,4-dimethoxyphenyl)ethan-1-one | HCID 270423 | — |
| Product | 2-(3,4-Dimethoxyphenyl)-7-methylimidazo(1,2-A)pyridine | HCID 9835127 | — |
Reaction Steps
The title compound, pale yellow solid, m.p. 163° C. and MS: m/e=268.1 (M+), was prepared in accordance with the general method of example 1 from 2-amino-4-methyl-pyridine and 3,4-dimethoxy-phenacylbromide.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06596731B2 |
| Source dataset | uspto-grants-2003_07 |
| ORD ID | ord-ffd1a6809b8d47468742888b1e8b47eb |
| Source note | uspto-grants-2003_07 |