HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethyl Acetoacetate → Ethyl 4-(5-fluoro-3',5'-bis(trifluoromethyl)-[1,1'-biphenyl]-2-yl)-6-methyl-2-(thiazol-2-yl)-1,4-dihydropyrimidine-5-carboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethyl Acetoacetate | HCID 8868 | — |
| Reactant | 1,3-Thiazole-2-carboximidamide hydrochloride | HCID 18679584 | — |
| Reactant | 5-Fluoro-3',5'-bis(trifluoromethyl)-[1,1'-biphenyl]-2-carbaldehyde | HCID 118107548 | — |
| Product | Ethyl 4-(5-fluoro-3',5'-bis(trifluoromethyl)-[1,1'-biphenyl]-2-yl)-6-methyl-2-(thiazol-2-yl)-1,4-dihydropyrimidine-5-carboxylate | HCID 118107590 | 26% |
Reaction Steps
5-fluoro-3′,5′-bis(trifluoromethyl)-[1,1′-biphenyl]-2-carbaldehyde (2.34 g, 6.96 mmol) was reacted with thiazole-2-carboximidamide hydrochloride (1.14 g, 6.96 mmol) and ethyl 3-oxobutanoate (1.1 g, 8.35 mmol) according to the procedure as described in Example 1, Step A to give the title compound as a yellow solid (1 g, 26%). 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-e1c714fa54394ee99195a31878898a02 |
| Source note | uspto-grants-2016_05 |