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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 378313Generated: October 29, 2026

HCID 19353526, compound → HCID 19353505, compound

https://huagongshe.com/reaction/378313

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 19353526HCID 19353526—
ReactantHCID 54480594HCID 54480594—
SolventEthanolHCID 702—
SolventMethylamineHCID 6329—
ProductHCID 19353505HCID 1935350570%

Reaction Steps

0.052 g (0.00015 mol) of 4-amino-N-(2-chloro-6-trifluoromethyl-pyridin-4-yl)-benzenesulfonamide was stirred in 30 ml of 8M methylamine in ethanol in an autoclave at 135° C. for 80 hours. The methylamine was allowed to evaporate, the residue was dissolved in ethanol, treated with 2 g of silica gel, concentrated and the residue was chromatographed on silica gel with ethyl acetate/hexane 1:2. There was obtained 0.036 g (70%) of 4-amino-N-(2-methylamino-6-trifluoromethyl-pyridin-4-yl)-benzenesulfonamide as colorless crystals; m.p.: >68° C. (dec.).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06030976
Source datasetuspto-grants-2000_02
ORD IDord-34e3ba44f7f54f2db45c0cf90b0e5757
Source noteuspto-grants-2000_02