HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methoxycarbonyl isothiocyanate → 4-Carbamoylthio-1,2-bis-(3-methoxycarbonyl-2-thioureido)-benzene
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methoxycarbonyl isothiocyanate | HCID 552246 | — |
| Reactant | 1-Amino-4-carbamoylthio-2-nitrobenzene | HCID 18949771 | — |
| Reactant | 1,2-Diamino-4-carbamoylthiobenzene | HCID 20371162 | — |
| Reactant | 4-Carbamoylthio-1-(3-methoxycarbonyl-2-thioureido)-2-nitrobenzene | HCID 20371172 | — |
| Solvent | Acetone | HCID 180 | — |
| Solvent | Iron | HCID 23925 | — |
| Product | 4-Carbamoylthio-1,2-bis-(3-methoxycarbonyl-2-thioureido)-benzene | HCID 20371224 | — |
Reaction Steps
In a similar manner, substituting 1-amino-4-carbamoylthio-2-nitrobenzene for the 4-carbamoylthio-1-(3-methoxycarbonyl-2-thioureido)-2-nitrobenzene in the iron reduction step, 1,2-diamino-4-carbamoylthiobenzene is prepared. 0.5 G. of this latter compound in 30 ml. acetone is treated overnight with 2 g. methoxy carbonyl isothiocyanate at room temperature. The solution is concentrated and the residue triturated with ether. Recrystallization yields 4-carbamoylthio-1,2-bis-(3-methoxycarbonyl-2-thioureido)-benzene.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04072696 |
| Source dataset | uspto-grants-1978_02 |
| ORD ID | ord-acd96665fa7d4ca0b5f857d9849ea754 |
| Source note | uspto-grants-1978_02 |