HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → N-cyano-N'-[2-[[[2-furanyl]methyl]thio]ethyl]-N"-methylguanidine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 1-Cyano-2,3-dimethylisothiourea | HCID 111103 | — |
| Reactant | 2-(Furfurylthio)ethylamine | HCID 118970 | — |
| Catalyst | Silver Nitrate | HCID 24470 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | N-cyano-N'-[2-[[[2-furanyl]methyl]thio]ethyl]-N"-methylguanidine | HCID 53954457 | 34.7% |
Reaction Steps
A solution of silver nitrate (8.25 g) in dimethylformamide (50 ml) was added dropwise to a solution of N-cyano-N'-methylcarbamimidothioic acid, methyl ester (6.1 g), triethylamine (4.8 g) and 2-[[[2-furanyl]methyl]thio]ethanamine (7.8 g) in methanol (150 ml). After 42 hr at 50° the mixture was filtered and the filtrate evaporated. The residue was partitioned between ethyl acetate and water. The organic layers were dried and evaporated to give an oil which yielded crystalline N-cyano-N'-[2-[[[2-furanyl]methyl]thio]ethyl]-N"-methylguanidine (3.9 g) m.p. 78°-82°.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04255440 |
| Source dataset | uspto-grants-1981_03 |
| ORD ID | ord-d90618d7bc064e32b1670504e857c360 |
| Source note | uspto-grants-1981_03 |