HuagongsheHuagongshe Chemistry Print Report · For research reference only
Guanidine → Trimethoprim
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Guanidine | HCID 3520 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | alpha-Carbethoxy-alpha-diethoxymethyl-beta-(3,4,5-trimethoxyphenyl)propionitrile | HCID 12559126 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | Trimethoprim | HCID 5578 | — |
Reaction Steps
A solution of α-carbethoxy-α-diethoxymethyl-β-(3,4,5-trimethoxyphenyl)propionitrile (7.9 g, 0.02 mol) and an equivalent amount of potassium hydroxide in ethanol (50 ml) was heated at reflux for one hour. A solution of guanidine (0.07 mol) in ethanol (50 ml) was added, and reflux was resumed. Some ethanol was allowed to boil off bringing the reaction temperature up to 85°. After about 20 hours at reflux the mixture was allowed to cool, and the product was filtered and washed with ethanol. The crude product was purified by treating with hot aqueous acetic acid and reprecipitation with ammonium hydroxide. The yield of purified trimethoprim (m.p. 197°-198°) was 3.6g (62%), its identity being confirmed by an NMR spectrum.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04144263 |
| Source dataset | uspto-grants-1979_03 |
| ORD ID | ord-e6a093a3d9a8427bba9ef92b52d464cf |
| Source note | uspto-grants-1979_03 |