HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethyl Acetoacetate → Ethyl 4-(2-bromo-4-fluorophenyl)-2-(5-methoxythiazol-2-yl)-6-methyl-1,4-dihydropyrimidine-5-carboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethyl Acetoacetate | HCID 8868 | — |
| Reactant | 2-Bromo-4-fluorobenzaldehyde | HCID 2773319 | — |
| Reactant | 5-Methoxythiazole-2-carboximidamide hydrochloride | HCID 90044391 | — |
| Product | Ethyl 4-(2-bromo-4-fluorophenyl)-2-(5-methoxythiazol-2-yl)-6-methyl-1,4-dihydropyrimidine-5-carboxylate | HCID 90042921 | 59% |
Reaction Steps
5-methoxythiazole-2-carboximidamide hydrochloride (3.3 g, 17 mmol) was reacted with 2-bromo-4-fluorobenzaldehyde (3.46 g, 17 mmol) and ethyl 3-oxobutanoate (2.2 g, 17 mmol) according to the procedure as described in Example 1, Step A to give the title compound as a yellow solid (4.56 g, 59%). The compound was characterized by the following spectroscopic data:
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09340538B2 |
| Source dataset | uspto-grants-2016_05 |
| ORD ID | ord-a2d81939c6d749d5b43453a6b057ad33 |
| Source note | uspto-grants-2016_05 |