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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1791133Generated: November 4, 2026

Triethylamine → HCID 22027868, compound

https://huagongshe.com/reaction/1791133

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantSulfuryl chlorideHCID 24648—
ReactantHCID 19689608HCID 19689608—
SolventTetrahydrofuranHCID 8028—
ProductHCID 22027868HCID 22027868—

Reaction Steps

A solution of sulfonyl chloride (0.63 g, 5.3 mmol) in THF (2 ml) is added within 5 minutes to a solution of 2-{4-(2-(3-chloro-phenylamino)-pyrimidin-4-yl]-pyridin-2-ylamino}-ethanol (1.50 g, 4.4 mmol) and triethylamine (3.0 ml, 22 mmol) in absolute THF (20 ml) at +5° C. After stirring the resulting suspension for four hours at room temperature it is partitioned between ethyl acetate and water. The organic phase is separated, dried over magnesium sulfate, filtered and evaporated under reduced presssure. The residue is purified by silicagel chromatography to give the title compound, m.p. 202–203° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07074787B2
Source datasetuspto-grants-2006_07
ORD IDord-71b823c546504e85b63e3a1e74f4dfa2
Source noteuspto-grants-2006_07