HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethyl 2-aminothiazole-4-carboxylate → Ethyl 2-amino-5-iodo-1,3-thiazole-4-carboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethyl 2-aminothiazole-4-carboxylate | HCID 73216 | — |
| Reactant | N-Iodosuccinimide | HCID 120273 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Sodium chloride; water | HCID 57417360 | — |
| Product | Ethyl 2-amino-5-iodo-1,3-thiazole-4-carboxylate | HCID 45117588 | 84% |
Reaction Steps
A solution of 14.53 g of 2-amino-4-ethoxycarbonylthiazole in 200 ml of THF was cooled in ice under an argon atmosphere, 20.0 g of N-iodosuccinimide was added to the cooled solution, and the mixture was stirred at the same temperature for 1.5 hr. Brine was added to the reaction solution, and the mixture was extracted with ethyl acetate. The organic layer was dried over anhydrous magnesium sulfate, was filtered, and was concentrated under the reduced pressure. The residue was purified by column chromatography on silica gel (hexane:ethyl acetate=1:1 to 1:2) to give 21.12 g of 2-amino-4-ethoxycarbonyl-5-iodothiazole.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07687490B2 |
| Source dataset | uspto-grants-2010_03 |
| ORD ID | ord-2787be1964134fb3bc3fa14307fa5693 |
| Source note | uspto-grants-2010_03 |