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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 610808Generated: October 31, 2026

Triethylamine → HCID 10640460, compound

https://huagongshe.com/reaction/610808

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantMethylamine hydrochlorideHCID 6364545—
ReactantHCID 10807034HCID 10807034—
SolventEthanolHCID 702—
ProductHCID 10640460HCID 1064046027%

Reaction Conditions

Temperature130 °C

Reaction Steps

0.20 g (0.00059 mol) of 4-amino-N-(2-azetidin-1-yl-6-chloro-pyrimidin-4-yl)-benzenesulfonamide was dissolved in 20 ml of ethanol, treated with 0.4 g (0.00588 mol) of methylamine hydrochloride and 2.28 ml (0.0176 mol) of triethylamine and stirred in an autoclave at 130° C. for 8 hours. The reaction mixture was freed from solvent and the residue was chromatographed on silica gel with methanol/dichloromethane 1:19. There was obtained 0.053 g (27%) of 4-amino-N-(2-azetidin-1-yl-6-methylamino-pyrimidin-4-yl)-benzenesulfonamide as light beige crystals; m.p.: >260° C. (dec.)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05998665
Source datasetuspto-grants-1999_12
ORD IDord-f79b2f9f01b94abba4ec57dfe2348662
Source noteuspto-grants-1999_12