HuagongsheHuagongshe Chemistry Print Report · For research reference only
Phenacyl bromide → 1-(5-Bromo-4-(4-phenylthiazol-2-yl)pyridin-2-yl)-3-ethylurea
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Phenacyl bromide | HCID 6259 | — |
| Reactant | AZD7118 Bromo Thioamide | HCID 59208439 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | 1-(5-Bromo-4-(4-phenylthiazol-2-yl)pyridin-2-yl)-3-ethylurea | HCID 59208504 | 84.7% |
Reaction Steps
To a mixture of 5-bromo-2-(3-ethylureido)pyridine-4-carbothioamide (Intermediate 42, 0.146 g, 0.48 mmol) in acetonitrile (3 mL), 2-bromo-1-phenylethanone (0.105 g, 0.53 mmol) was added and the reaction mixture was heated to 80° for 16 h. The reaction mixture was cooled to room temperature and concentrated under reduced pressure. The resulting solids were filtered and washed with acetonitrile to yield 164 mg of the title compound as an off-white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07674801B2 |
| Source dataset | uspto-grants-2010_03 |
| ORD ID | ord-5f795704f2194ca29e815cfebf151739 |
| Source note | uspto-grants-2010_03 |