HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethyl isothiocyanatoformate → 1-Ethoxycarbonyl-3-(2-dimethylaminoacetamidophenyl)thiourea
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethyl isothiocyanatoformate | HCID 85320 | — |
| Reactant | N-(2-aminophenyl)-2-(dimethylamino)acetamide | HCID 16784338 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | 1-Ethoxycarbonyl-3-(2-dimethylaminoacetamidophenyl)thiourea | HCID 21482982 | 62.9% |
Reaction Steps
A suspension of N-(2-aminophenyl)-2-dimethylaminoacetamide (8.9 g) (prepared as described in Example 6) in acetonitrile (50 ml) was treated with ethoxycarbonyl isothiocyanate (6.4 g), dropwise with stirring, maintaining the temperature at 15°-20° C. by external cooling. When the addition was complete, the solid had dissolved but after being left to stand for a further 5 minutes, another solid precipitated. This was filtered off and washed with ice-cold acetonitrile to give 1-ethoxycarbonyl-3-(2-dimethylaminoacetamidophenyl)thiourea (9.4 g), m.p. 159°-160° C. (with decomposition).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04005217 |
| Source dataset | uspto-grants-1977_01 |
| ORD ID | ord-dad36edf293c4c5eaabc06dca4f775b0 |
| Source note | uspto-grants-1977_01 |