HuagongsheHuagongshe Chemistry Print Report · For research reference only
Guanidine → HCID 18927266, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Guanidine | HCID 3520 | — |
| Reactant | Thiophenol | HCID 7969 | — |
| Reactant | HCID 10517570 | HCID 10517570 | — |
| Reactant | HCID 18927300 | HCID 18927300 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Triethylamine | HCID 8471 | — |
| Product | HCID 18927266 | HCID 18927266 | — |
Reaction Steps
A suspension of 1 g of N-diaminomethylene-2-methyl-4-chloro-5-methylsulfonylbenzamide [obtainableby reaction of 2-methyl-4-chloro-5-methylsulfonylbenzoyl chloride with guanidine in the presence of triethylamine], 7 ml of thiophenol and 6 g ofK2CO3 is heated at 180° for 90 min. It is dissolved in water and extracted with ethyl acetate, and the extract is evaporated. N-Diaminomethylene-2-methyl-4-(2-methylphenylthio)-5-methylsulfonylbenzamide is obtained, from which, after treatment with 1.5 g of sodium perborate in 30 ml of glacial acetic acid over a period of 2 hours at 60° C. in a water bath, N-diaminomethylene-2-methyl-4-(2-methylphenylsulfonyl)-5methylsulfonylbenzamide is obtained after customary working up.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05744641 |
| Source dataset | uspto-grants-1998_04 |
| ORD ID | ord-a9bae023ce4947098dd08585511b340e |
| Source note | uspto-grants-1998_04 |