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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1802182Generated: October 25, 2026

O-(2,4,6-Trimethylbenzenesulfonyl)hydroxylamine → 1,2-Diamino-5-fluoro-4-(methoxycarbonyl)pyridinium 2,4,6-trimethylbenzenesulfonate

https://huagongshe.com/reaction/1802182

Reaction equation

Participants

RoleNameHCIDCharge
ReactantO-(2,4,6-Trimethylbenzenesulfonyl)hydroxylamineHCID 11830845—
ReactantMethyl 2-amino-5-fluoroisonicotinateHCID 67777217—
SolventDiethyl EtherHCID 3283—
SolventDichloromethaneHCID 6344—
Product1,2-Diamino-5-fluoro-4-(methoxycarbonyl)pyridinium 2,4,6-trimethylbenzenesulfonateHCID 8666601881.4%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08349824B2
Source datasetuspto-grants-2013_01
ORD IDord-73fd0b8537fd408da9189c55c488073f
Source noteuspto-grants-2013_01