HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Chlorobenzaldehyde → Ethyl 4-(2-chlorophenyl)-6-methyl-2-(thiazol-2-yl)-1,4-dihydropyrimidine-5-carboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Chlorobenzaldehyde | HCID 6996 | — |
| Reactant | Ethyl Acetoacetate | HCID 8868 | — |
| Reactant | 1,3-Thiazole-2-carboximidamide hydrochloride | HCID 18679584 | — |
| Product | Ethyl 4-(2-chlorophenyl)-6-methyl-2-(thiazol-2-yl)-1,4-dihydropyrimidine-5-carboxylate | HCID 9841888 | 55.2% |
Reaction Steps
Thiazole-2-carboximidamide hydrochloride (11.63 g, 71.1 mmol) was reacted with 2-chlorobenzaldehyde (10 g, 71.1 mmol) and ethyl 3-oxobutanoate (11.1 g, 85.3 mmol) according to the procedure as described in Example 1, Step A to give the title compound as a yellow solid (14.2 g, 55%). 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-20e8d0bf90024350afec12e92f972990 |
| Source note | uspto-grants-2016_05 |