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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2199319Generated: October 26, 2026

3-Iodophenol → (E)-tert-butyl 4-(4-(5-(3-hydroxystyryl)pyrazin-2-ylamino)phenylsulfonyl)piperazine-1-carboxylate

https://huagongshe.com/reaction/2199319

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-IodophenolHCID 12272—
ReactantPhosphine, tris(4-methylphenyl)-HCID 13956—
ReactantDiisopropylethylamineHCID 81531—
ReactantTert-butyl 4-(4-(5-vinylpyrazin-2-ylamino)phenylsulfonyl)piperazine-1-carboxylateHCID 67324584—
Catalystpalladium(II) acetateHCID 167845—
SolventDimethylformamideHCID 6228—
Product(E)-tert-butyl 4-(4-(5-(3-hydroxystyryl)pyrazin-2-ylamino)phenylsulfonyl)piperazine-1-carboxylateHCID 6732568878.5%

Reaction Conditions

Temperature120 °C

Reaction Steps

A mixture of tert-butyl 4-(4-(5-vinylpyrazin-2-ylamino)phenylsulfonyl)piperazine-1-carboxylate (40 mg, 0.09 mmol), 3-iodophenol (19 mg, 0.09 mmol), Pd(OAc)2 (1.2 mg, 0.005 mmol), tri-p-tolylphosphine (2.5 mg, 0.008 mmol), and DIEA (31 μL, 0.18 mmol) in DMF (3 ml) was heated at 120° C. for 18 h after which, it was filtered with a pad of celite and partitioned between ethyl acetate and water. The organic layer was separated and the aqueous layer was extracted with ethyl acetate. The combined organic extracts were washed with brine, dried over MgSO4, celite filtered and concentrated under reduced pressure. The crude product was purified by flash chromatography using (20% to 40% Ethyl acetate/Hexane) as a solvent to afford title compound (38 mg, 78% yield). MS m/z: 538 [M+1].

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09358231B2
Source datasetuspto-grants-2016_06
ORD IDord-c9e2b722eff441f182baf5bc824f27f7
Source noteuspto-grants-2016_06