HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methyl iodide → 5-[(E)-C-[2-(4-bromophenyl)-2-(4-methyl-1,3-thiazol-5-yl)ethyl]-N-hydroxycarbonimidoyl]-1-methylpyridin-2-one
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Hydroxyamine hydrochloride | HCID 443297 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | 5-(3-(4-bromophenyl)-3-(4-methylthiazol-5-yl)propanoyl)pyridin-2(1H)-one | HCID 66668555 | — |
| Product | 5-[(E)-C-[2-(4-bromophenyl)-2-(4-methyl-1,3-thiazol-5-yl)ethyl]-N-hydroxycarbonimidoyl]-1-methylpyridin-2-one | HCID 58043504 | — |
Reaction Steps
In analogy to example 161, step 1, 5-(3-(4-bromophenyl)-3-(4-methylthiazol-5-yl)propanoyl)pyridin-2(1H)-one was reacted with iodomethane in the presence of potassium carbonate. The product of this reaction was reacted in analogy to example 151, step 3 with hydroxylamine hydrochloride in the presence of sodium hydrogencarbonate to give the title compound containing less than 10% of the corresponding Z isomer as an off-white solid, MS (ESI+): m/z=432.1 [M+H]+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08765730B2 |
| Source dataset | uspto-grants-2014_07 |
| ORD ID | ord-b268511d744741cb88d4c5edfaab2a8e |
| Source note | uspto-grants-2014_07 |