HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ammonium Hydroxide → Ethyl 2-amino-4-(propan-2-yl)-1,3-thiazole-5-carboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ammonium Hydroxide | HCID 14923 | — |
| Reactant | Thiourea | HCID 2723790 | — |
| Reactant | Ethyl 2-bromo-4-methyl-3-oxopentanoate | HCID 13015595 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | Ethyl 2-amino-4-(propan-2-yl)-1,3-thiazole-5-carboxylate | HCID 824436 | 66.4% |
Reaction Steps
To a refluxing solution of thiourea (1.9 g, 25.6 mmol) in absolute ethanol (20 mL) was added ethyl 2-bromo-4-methyl-3-oxopentanoate (6.0 g, 25.3 mmol). The solution was stirred at reflux for another 1.5 hours. After cooling to room temperature, the solution was poured in ice/water (100 mL). The mixture was neutralized with concentrated NH4OH. The solid material was recovered by filtration, washed with water (2×20 mL) and hexanes (2×20 mL), and dried in vacuo, affording ethyl 2-amino-4-(propan-2-yl)-1,3-thiazole-5-carboxylate (3.6 g, 66% yield). The product was used without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09315521B2 |
| Source dataset | uspto-grants-2016_04 |
| ORD ID | ord-410d14fa27b041738e27adb1a732b1e8 |
| Source note | uspto-grants-2016_04 |