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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 610834Generated: November 1, 2026

Ethylamine → HCID 19353515, compound

https://huagongshe.com/reaction/610834

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthylamineHCID 6341—
ReactantHCID 10689660HCID 10689660—
ProductHCID 19353515HCID 193535152.5%

Reaction Steps

2.5 g (0.007 mol) of 4-amino-N-(2-bromo-6-methylamino-pyridin-4-yl)-benzenesulfonamide were stirred with 80 ml of ethylamine in an autoclave at 160° C. for 40 hours. The residual ethylamine was left to evaporate and the residue was chromatographed on silica gel with ethyl acetate/hexane 1:2, then 2:3 and finally 1:1. The thus-obtained 0.67 g of brown oil was suspended in 200 ml of 1N NaOH, suction filtered and the filtrate was neutralized with 1N HCl. It was again suction filtered, the filtrate was saturated with NaCl and extracted with ethyl acetate. The organic phase was dried. There was obtained 0.055 g (2.5%) of 4-amino-N-(2-ethylamino-6-methylamino-pyridin-4-yl)-benzenesulfonamide as pale brown crystals; MS (ISN): me/e=320 (C14H18N5O2S-).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05998665
Source datasetuspto-grants-1999_12
ORD IDord-81767fa9438b46739971a081f65cc278
Source noteuspto-grants-1999_12