HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydroxyamine hydrochloride → N-hydroxy-3-((2-phenylimidazo[1,2-a]pyridin-3-yl)-methyl)-1,2,4-oxadiazole-5-carboxamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydroxyamine hydrochloride | HCID 443297 | — |
| Reactant | HCID 44539338 | HCID 44539338 | — |
| Reactant | HCID 67028744 | HCID 67028744 | — |
| Product | N-hydroxy-3-((2-phenylimidazo[1,2-a]pyridin-3-yl)-methyl)-1,2,4-oxadiazole-5-carboxamide | HCID 86655128 | — |
Reaction Steps
The title compound was prepared in the same fashion as that for compound 222 from ethyl 3-((2-(4-chlorophenyl)imidazo[1,2-a]pyridin-3-yl)methyl)-1,2,4-oxadiazole-5-carboxylate and hydroxylamine hydrochloride. m/e+=370 (M+H+). 1H NMR (400 MHz, in DMSO-d6): δ 8.43-8.41 (1H, D, d, J=7.2 Hz, ArH), δ 8.31 (1H, D, s, ArH), δ 7.88-7.86 (2H, D, d, J=8.4 Hz, ArH), δ 7.65-7.62 (1H, D, d, J=9.2 Hz, ArH), δ 7.57-7.54 (1H, D, d, J=8.4 Hz, ArH), δ 7.35-7.31 (1H, D, t, J=8.0, ArH), δ 7.04-7.00 (1H, D, t, J=8.0, ArH), and δ 4.62 (2H, D, s, CH2).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08497278B2 |
| Source dataset | uspto-grants-2013_07 |
| ORD ID | ord-2ec0d0a4d83746d0ab3255cfd83f2ee2 |
| Source note | uspto-grants-2013_07 |