HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Aminopyridine → 2-(3,4-Dimethoxyphenyl)imidazo[1,2-a]pyridine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Aminopyridine | HCID 10439 | — |
| Reactant | 2-Bromo-1-(3,4-dimethoxyphenyl)ethan-1-one | HCID 270423 | — |
| Product | 2-(3,4-Dimethoxyphenyl)imidazo[1,2-a]pyridine | HCID 659246 | — |
Reaction Steps
The title compound, pale yellow solid, m.p. 96° C. and MS: m/e=254.1 (M+), was prepared in accordance with the general method of example 1 from 2-amino-pyridine and 3,4-dimethoxy-phenacylbromide.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06861437B2 |
| Source dataset | uspto-grants-2005_03 |
| ORD ID | ord-e2f11957528540f88db86216ceb9abfe |
| Source note | uspto-grants-2005_03 |