HuagongsheHuagongshe Chemistry Print Report · For research reference only
Guanidine → Ormetoprim
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Guanidine | HCID 3520 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | HCID 12559127 | HCID 12559127 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | Ormetoprim | HCID 23418 | — |
Reaction Steps
A solution of α-carbethoxy-α-diethoxymethyl-β-(4,5-dimethoxy-2-methylphenyl)propionitrile (3.9 g, 0.01 mol) and an equivalent amount of potassium hydroxide in ethanol (70 ml) was heated at reflux for one hour. A solution of guanidine (0.035 mol) in ethanol (50 ml) was added, and reflux was resumed. Ethanol was boiled off until the reaction temperature reached 85° C. After 20 hours at reflux the mixture was allowed to cool, and the product was filtered and washed with ethanol giving 2.57 g (94%) of nearly white solid. After purification as described in Example 5, the product was dried under reduced pressure giving a white solid, m.p. 231°-233° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04144263 |
| Source dataset | uspto-grants-1979_03 |
| ORD ID | ord-bfbea14066cc486ab05c9426d8e411ef |
| Source note | uspto-grants-1979_03 |