HuagongsheHuagongshe Chemistry Print Report · For research reference only
3-Benzyl-1-methylthiourea → 2-Benzylimino-4-(4-chloro-3-sulfamoylphenyl)-3-methyl-1,3-thiazolidine-4-ol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 3-Benzyl-1-methylthiourea | HCID 2735489 | — |
| Reactant | Bromo-4'-chloro-3'-sulfamoylacetophenone | HCID 12952390 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | 2-Benzylimino-4-(4-chloro-3-sulfamoylphenyl)-3-methyl-1,3-thiazolidine-4-ol | HCID 22760594 | — |
Reaction Steps
4.7 g of 2-bromo-4'-chloro-3'-sulfamoylacetophenone and 2.7 g of 1-benzyl-3-methylthiourea were reacted as prescribed in Example 23 and the reaction mixture was introduced into 200 ml of diethyl ether while stirring. The hygroscopic crystals of the 2-benzylimino-4-(4-chloro-3-sulfamoylphenyl)-3-methyl-1,3-thiazolidine-4-ol-hydrobromide were rapidly filtered off, dissolved in 70 ml of water and converted into the end product according to the prescription of Example 28. Colorless solid body: decomposition beginning at 110° C, γC=N 1610 cm-1.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04061761 |
| Source dataset | uspto-grants-1977_12 |
| ORD ID | ord-636ab6baacaa43cb8fcd008e530617f3 |
| Source note | uspto-grants-1977_12 |