HuagongsheHuagongshe Chemistry Print Report · For research reference only
Aniline → HCID 178511995, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Aniline | HCID 6115 | — |
| Reactant | HCID 9794880 | HCID 9794880 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 178511995 | HCID 178511995 | — |
Reaction Steps
0.26 g of 6-chloro-8H-indeno[1,2-d]thiazol-2-yl-cyanamide is suspended in 10 ml of ethanol at room temperature and, after addition of 0.1 of aniline, heated to reflux for 6 h. The reaction mixture is concentrated in vacuo, and the residue is purified by chromatography on silica gel with 5/1 dichloromethane/ethyl acetate. N-(6-Chloro-8H-indeno[1,2-d]thiazol-2-yl)-N′-phenylguanidine is obtained and melts with decomposition at 210° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06476059B1 |
| Source dataset | uspto-grants-2002_11 |
| ORD ID | ord-79a38a5a568b459698f97898d134371a |
| Source note | uspto-grants-2002_11 |