HuagongsheHuagongshe Chemistry Print Report · For research reference only
O-(2,4,6-Trimethylbenzenesulfonyl)hydroxylamine → 1,2-Diamino-5-fluoro-4-(methoxycarbonyl)pyridinium 2,4,6-trimethylbenzenesulfonate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | O-(2,4,6-Trimethylbenzenesulfonyl)hydroxylamine | HCID 11830845 | — |
| Reactant | Methyl 2-amino-5-fluoroisonicotinate | HCID 67777217 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 1,2-Diamino-5-fluoro-4-(methoxycarbonyl)pyridinium 2,4,6-trimethylbenzenesulfonate | HCID 86666018 | 81.4% |
Reaction Steps
To an ice-cooled white suspension of O-(mesitylsulfonyl)hydroxylamine (1.18 g, 5.48 mmol) in dichloromethane (8.44 ml) is added dropwise a solution of methyl 2-amino-5-fluoroisonicotinate (932 mg, 5.48 mmol) in dichloromethane (2.53 ml). The resulting light brown suspension is stirred for 2 hours at room temperature. The suspension is cooled to −5-0° C., diluted with diethylether (15 ml) and stirred for 30 minutes. The solid is collected by filtration, washed with diethyl ether and dried affording 1,2-diamino-5-fluoro-4-(methoxycarbonyl)pyridinium 2,4,6-trimethylbenzenesulfonate (1.72 g, 81.4%) as a light brown solid. MS: m/z=186.0 (M+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08349824B2 |
| Source dataset | uspto-grants-2013_01 |
| ORD ID | ord-73fd0b8537fd408da9189c55c488073f |
| Source note | uspto-grants-2013_01 |