HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Amino-5-chlorobenzenesulphonamide → 4'-(2-Dimethylaminoethyl)-7-chlorospiro[2H-1,2,4-benzothiadiazine-3(4H),1'-cyclohexane]-1,1-dioxide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Amino-5-chlorobenzenesulphonamide | HCID 12295550 | — |
| Reactant | 4-(2-Dimethylaminoethyl)cyclohexanone | HCID 23337786 | — |
| Solvent | Hydrochloric Acid | HCID 313 | — |
| Product | 4'-(2-Dimethylaminoethyl)-7-chlorospiro[2H-1,2,4-benzothiadiazine-3(4H),1'-cyclohexane]-1,1-dioxide | HCID 23337783 | — |
Reaction Steps
A mixture of 2-amino-5-chlorobenzenesulfonamide (8.0 g., 0.039 mole) and 4-(2-dimethylaminoethyl)cyclohexanone (13.5 g., 0.08 mole) in 0.6 N ethanolic HCl (110 ml.) is heated at reflux 18 hours. The solvent is evaporated at reduced pressure and the residue dissolved in water (100 ml.) and neutralized with sodium hydroxide to precipitate 4'-(2-dimethylaminoethyl)-7-chlorospiro-[2H-1,2,4-benzothiadiazine-3(4H),1'-cyclohexane]-1,1-dioxide hemisemihydrate which melts at 234°-5° C. after recrystallization from n-propanol.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04226867 |
| Source dataset | uspto-grants-1980_10 |
| ORD ID | ord-2d2a3a964fa44afc9bb5b120a155b634 |
| Source note | uspto-grants-1980_10 |