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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1584218Generated: November 2, 2026

Ethylamine → HCID 19353515, compound

https://huagongshe.com/reaction/1584218

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 numberUS05932599
Source datasetuspto-grants-1999_08
ORD IDord-014bfd2d448e45d3babe39710171320d
Source noteuspto-grants-1999_08