HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-Amidinobenzamide Hydrochloride → 4-[5-(4-Cyanophenyl)-2-pyrimidinyl]benzamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-Amidinobenzamide Hydrochloride | HCID 2724293 | — |
| Reactant | Sodium | HCID 5360545 | — |
| Reactant | 2-(4-Cyanophenyl)-3-methoxyacrolein | HCID 54100265 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 4-[5-(4-Cyanophenyl)-2-pyrimidinyl]benzamide | HCID 18991914 | — |
Reaction Steps
247 mg of sodium are treated at room temperature with 10 ml of methanol. After 15 minutes the solution obtained is treated at room temperature with 1.58 g of 4-amidinobenzamide hydrochloride. A white suspension forms and this is treated dropwise at room temperature within 10 minutes with a solution of 1.42 g of 2-(4-cyanophenyl)-3-methoxyacrolein in 50 ml of methanol. The reaction mixture is stirred at room temperature for a further 2 hours and then suction filtered. The residue is washed with water, tetrahydrofuran and diethyl ether and dried in a high vacuum. 4-[5-(4-Cyanophenyl)-2-pyrimidinyl]benzamide is obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05486310 |
| Source dataset | uspto-grants-1996_01 |
| ORD ID | ord-f2c4875e63134ec497c2dfd574b7b513 |
| Source note | uspto-grants-1996_01 |