HuagongsheHuagongshe Chemistry Print Report · For research reference only
HCID 21433222, compound → HCID 178527179, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | HCID 21433222 | HCID 21433222 | — |
| Reactant | Ethylorthoformate | HCID 53630039 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | HCID 178527179 | HCID 178527179 | 91.5% |
Reaction Steps
A mixture of 6 g 2-amino-4-trifluoromethyl-5-fluoro-benzenesulfonamide, m.p.= 152° C. (formula V: R2 = F) and 18 g ethyl orthoformate is heated at 120°-125° C., during 30 minutes to one hour, in an open vessel. After cooling, the reaction mixture is diluted with 150 ml dry diethyl ether. The resulting precipitate is collected and recrystallized from aqueous ethanol, to give 5.7 g of 6-trifluoromethyl-7-fluoro-2H-1,2,4-benzothiadiazine-1,1-dioxide, M.p.= 234° C. B. Action of formic acid
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04025508 |
| Source dataset | uspto-grants-1977_05 |
| ORD ID | ord-72d6b224b92444f7a9686cc1f621864b |
| Source note | uspto-grants-1977_05 |