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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 378306Generated: October 29, 2026

Ethylamine → HCID 19353515, compound

https://huagongshe.com/reaction/378306

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 numberUS06030976
Source datasetuspto-grants-2000_02
ORD IDord-1f22027a6cb4455ab072b1ff0bd78609
Source noteuspto-grants-2000_02