HuagongsheHuagongshe Chemistry Print Report · For research reference only
Formamide → N-cyano-N'-[2-(3-formylamino-2-oxobutylthio)ethyl]-N"-methylguanidine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Formamide | HCID 713 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | Sodium Formate | HCID 2723810 | — |
| Reactant | Ammonium formate | HCID 2723923 | — |
| Reactant | N-[2-(2-chloro-3-oxobutylthio)ethyl]-N'-cyano-N"-methylguanidine | HCID 14153741 | — |
| Product | N-cyano-N'-[2-(3-formylamino-2-oxobutylthio)ethyl]-N"-methylguanidine | HCID 14457222 | 19% |
Reaction Steps
In 2.5 ml of formamide were dissolved 131 mg of N-[2-(2-chloro-3-oxobutylthio)ethyl]-N'-cyano-N"-methylguanidine, 136 mg of sodium formate and 320 mg of ammonium formate, and the solution was stirred at room temperature for 3 days. Then, 420 mg of sodium hydrogencarbonate was added to the solution and formamide was removed under reduced pressure, and the obtained residue was refined by silica gel column chromatography (developing solvent: chloroform/ethanol=5/1) to obtain 28 mg of a colorless oily product (the yield was 19%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04886910 |
| Source dataset | uspto-grants-1989_12 |
| ORD ID | ord-bef66331277f4ed6b63d2b7c21f53649 |
| Source note | uspto-grants-1989_12 |