HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetamidine monohydrochloride → N-[[(3-Chloro-4-cyanophenyl)amino]carbonyl]ethanimidamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetamidine monohydrochloride | HCID 67170 | — |
| Reactant | Sodium | HCID 5360545 | — |
| Reactant | HCID 19852150 | HCID 19852150 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | N-[[(3-Chloro-4-cyanophenyl)amino]carbonyl]ethanimidamide | HCID 152746157 | — |
Reaction Steps
Following a procedure similar to that described in Example 1 but using 2.06 g. sodium in 250 ml. dry acetone, 9.2 g. acetamidine hydrochloride and 16 g. 3-chloro-4-cyanophenyl isocyanate in 250 ml. dry acetone, there was obtained after filtration of the reaction mixture a solid which on washing with water and recrystallization from methyl alcohol gave 1-(3-chloro-4-cyanophenyl)3 -(acetimidoyl)urea; m.p.182°-183°C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US03984467 |
| Source dataset | uspto-grants-1976_10 |
| ORD ID | ord-faecb4f338be43b48d05f54cf25f4293 |
| Source note | uspto-grants-1976_10 |