HuagongsheHuagongshe Chemistry Print Report · For research reference only
N,N-Dimethylcyclohexylamine → HCID 13246819, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | N,N-Dimethylcyclohexylamine | HCID 7415 | — |
| Reactant | Benzenebutanol | HCID 76889 | — |
| Reactant | 2H-1,2,4,6-Thiatriazine, 3-chloro-5-methoxy-2-methyl-, 1,1-dioxide | HCID 157195 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 13246819 | HCID 13246819 | — |
Reaction Steps
A mixture of 27 parts of 4-phenyl-n-butanol with 23 parts of N,N-dimethylcyclohexylamine, and 31.7 parts of 5-chloro-6-methyl-3-methoxy-6H-1,2,4,6-thiatriazine-1,1-dioxide, were added side by side, in the course of 15 minutes, to 250 parts of methylene chloride at from 10° to 15° C., while stirring. Stirring was continued for one hour at room temperature, after which the reaction mixture was washed with 1N hydrochloric acid and with 10% strength sodium carbonate solution, and dried over magnesium sulfate. After evaporating down under reduced pressure, 40 parts of the 6-methyl-3-methoxy-5-(4-phenylbutoxy)-6H-1,2,4,6-thiatriazine-1,1-dioxide of melting point 74°-78° C. were obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04472191 |
| Source dataset | uspto-grants-1984_09 |
| ORD ID | ord-79d2bad0cfca41a9a4ba7be919797062 |
| Source note | uspto-grants-1984_09 |