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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1584192Generated: November 2, 2026

Ethylamine → HCID 17774540, compound

https://huagongshe.com/reaction/1584192

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthylamineHCID 6341—
ReactantHCID 10807034HCID 10807034—
SolventEthanolHCID 702—
ProductHCID 17774540HCID 1777454044%

Reaction Conditions

Temperature130 °C

Reaction Steps

0.2 g (0.00061 mol) of 4-amino-N-(2-azetidin-1-yl-6-chloro-pyrimidin-4-yl)-benzenesulfonamide was dissolved in 20 ml of ethanol, treated with 3.9 ml (0.061 mol) of ethylamine and stirred in an autoclave at 130° C. for 12 hours. The reaction mixture was free from solvent, the residue was suspended in 5 ml of ethanol and treated in an ultrasound bath for 15 minutes. The precipitate was filtered off, dissolved in 10 ml of 0.1N NaOH and filtered. The filtrate was adjusted to pH 6 with 0.1N HCl. The precipitate was filtered off under suction, washed with water and dried. There was obtained 0.090 g (44%) of 4-amino-N-(2-azetidin-1-yl-6-ethylamino-pyrimidin-4-yl)-benzenesulfonamide as beige crystals; m.p.: 260-262° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05932599
Source datasetuspto-grants-1999_08
ORD IDord-d0d5f2a246554f31bbeb6f7089f72ae5
Source noteuspto-grants-1999_08