HuagongsheHuagongshe Chemistry Print Report · For research reference only
3-[3-(Pyridin-3-yl)phenyl]imidazo[1,2-alpha]pyridine-7-carboxaldehyde → 3-[3-(Pyridin-3-yl)phenyl]imidazo[1,2-alpha]pyridine-7-carboxaldehyde O-(2-dimethylaminoethyl)oxime
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 3-[3-(Pyridin-3-yl)phenyl]imidazo[1,2-alpha]pyridine-7-carboxaldehyde | HCID 9944128 | — |
| Reactant | Dimethylaminoethoxyamine hydrochloride | HCID 21928691 | — |
| Product | 3-[3-(Pyridin-3-yl)phenyl]imidazo[1,2-alpha]pyridine-7-carboxaldehyde O-(2-dimethylaminoethyl)oxime | HCID 131724805 | — |
Reaction Steps
The title compound was prepared in a similar manner to that described in Example 14 using O-(2-dimethylaminoethyl)hydroxylamine hydrochloride and 3-[3-(pyridin-3-yl)phenyl]imidazo[1,2-α]pyridine-7-carboxaldehyde to afford a brown oil, essentially as a single geometric isomer. 1H NMR (400 MHz, CDCl3) δH 2.97 (6H, s), 3.43-3.47 (2H, m), 4.65-4.69 (2H, m), 7.28-7.33 (2H, m), 7.42-7.47 (1H, m), 7.62-7.82 (4H, m), 7.94-7.98 (1H, m), 8.20 (1H, s), 8.32-8.35 (1H, m), 8.25 (1H, s), 8.61-8.65(1H, m), 8.90 (1H, s); m/z (ES+) 386 (M++H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06872731B2 |
| Source dataset | uspto-grants-2005_03 |
| ORD ID | ord-25983a5ea2bc4eb69659bc675b6207b9 |
| Source note | uspto-grants-2005_03 |