HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium Iodide → 1-Thioacetylmethyl-2-nitroimidazole
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium Iodide | HCID 5238 | — |
| Reactant | 2-Nitroimidazole | HCID 10701 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | Chloromethylthioacetate | HCID 53833355 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | 1-Thioacetylmethyl-2-nitroimidazole | HCID 86656269 | — |
Reaction Steps
To a solution of the chloromethylthioacetate in MeCN (100 mL) was added 2-nitroimidazole (3 g), NaI (1 g) and diisopropylethyl amine (DIEA) and refluxed. A precipitate formed after 3 h. Additional DIEA (3 mL) was added to the reaction mixture and refluxed for 4 h. Volatiles were removed, EtOAc (300 mL) added to the residue, and the ensuing mixture filtered. The filtrate was washed with water, 1M aqueous citric acid, brine, and concentrated to yield a residue. The residue was separated by column chromatography using 0-90% EtOAc/Hexane as eluent to yield 1-thioacetylmethyl-2-nitroimidazole (vi, 3.15 g) that was chlorinated as described above in Example 1A to yield compound vii.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08309554B2 |
| Source dataset | uspto-grants-2012_11 |
| ORD ID | ord-8296122d7f0340a3a24c6d0c5a488814 |
| Source note | uspto-grants-2012_11 |