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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1876560Generated: November 2, 2026

Hydroxybenzenesulfonic acid → 5-{8-[(3R)-4-acetyl-3-methylpiperazin-1-yl]-6-morpholin-4-yl-9-(2,2,2-trifluoroethyl)-9H-purin-2-yl}pyrimidin-2-amine benzenesulfonate

https://huagongshe.com/reaction/1876560

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydroxybenzenesulfonic acidHCID 15619088—
ReactantDs-7423HCID 45378170—
SolventEthanolHCID 702—
Product5-{8-[(3R)-4-acetyl-3-methylpiperazin-1-yl]-6-morpholin-4-yl-9-(2,2,2-trifluoroethyl)-9H-purin-2-yl}pyrimidin-2-amine benzenesulfonateHCID 8634419067%

Reaction Steps

To a suspension of 5-{8-[(3R)-4-acetyl-3-methylpiperazin-1-yl]-6-morpholin-4-yl-9-(2,2,2-trifluoroethyl)-9H-purin-2-yl}pyrimidin-2-amine (126 mg, 0.242 mmol) in 10% aqueous ethanol solution (5 ml) was added benzenesulfonic acid mono hydrate (46.8 mg, 0.266 mmol) at 50° C., and the mixture was allowed to be cooled down to room temperature, and stirred for 15 hr. The solid precipitated out was collected and dried to give 5-{8-[(3R)-4-acetyl-3-methylpiperazin-1-yl]-6-morpholin-4-yl-9-(2,2,2-trifluoroethyl)-9H-purin-2-yl}pyrimidin-2-amine benzenesulfonate (110 mg) as a yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08309546B2
Source datasetuspto-grants-2012_11
ORD IDord-d902ef6effed4f12abf8ce29f0c8574f
Source noteuspto-grants-2012_11