HuagongsheHuagongshe Chemistry Print Report · For research reference only
3-[3-(7-Formylimidazo[1,2-alpha]pyridin 3-yl)phenyl]thiophene-2-carbonitrile → 3-[3-(7-(2-Dimethylaminoethoxy)iminomethylimidazo[1,2-alpha]pyridin-3-yl)phenyl]thiophene-2-carbonitrile
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 3-[3-(7-Formylimidazo[1,2-alpha]pyridin 3-yl)phenyl]thiophene-2-carbonitrile | HCID 9902013 | — |
| Reactant | Dimethylaminoethoxyamine hydrochloride | HCID 21928691 | — |
| Product | 3-[3-(7-(2-Dimethylaminoethoxy)iminomethylimidazo[1,2-alpha]pyridin-3-yl)phenyl]thiophene-2-carbonitrile | HCID 85331392 | — |
Reaction Steps
The title compound was prepared in a similar manner to that described in Example 14 using O-(2-dimethylaminoethyl)hydroxylamine hydrochloride (144 mg, 0.82 mmol) and 3-[3-(7-formylimidazo[1,2-α]pyridin-3-yl)phenyl]thiophene-2-carbonitrile (90 mg, 0.27 mmol) to afford a yellow solid (42 mg, 38%), essentially as a single geometric isomer, m.p. 74-75° C. 1H NMR (360 MHz, CDCl3) δH 2.33 (6H, s), 2.67-2.71 (2H, m), 4.30-4.34 (2H, m), 7.33-7.37 (2H, m), 7.63-7.70 (4H, m), 7.79 (1H, s), 7.91 (1H, s), 8.15 (1H, s), 8.45 (1H, d, J 7); m/z (ES+) 416 (M++H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06872731B2 |
| Source dataset | uspto-grants-2005_03 |
| ORD ID | ord-38be777e8e764f90b2b439cf543c68ef |
| Source note | uspto-grants-2005_03 |