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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1027218Generated: October 30, 2026

Iodo benzene diacetate → HCID 136377151, compound

https://huagongshe.com/reaction/1027218

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodo benzene diacetateHCID 12217721—
ReactantHCID 86710620HCID 86710620—
Catalystpalladium(II) acetateHCID 167845—
SolventAcetic AcidHCID 176—
SolventAcetic AnhydrideHCID 7918—
ProductHCID 136377151HCID 136377151—

Reaction Conditions

Temperature60 °C

Reaction Steps

A mixture of 4-(6-(methyl(2,2,6,6-tetramethylpiperidin-4-yl)amino)pyridazin-3-yl)-3-(trifluoromethoxy)phenyl trifluoromethanesulfonate (360 mg, 0.647 mmol), iodobenzene diacetate (375 mg, 1.164 mmol) and Pd(OAc)2 (7.3 mg, 0.032 mmol) in AcOH (3.0 mL) and Ac2O (3.0 mL) was heated at 60° C. overnight. The reaction mixture was cooled to room temperature and concentrated. The residue was basified with aqueous NaHCO3 solution and extracted with DCM. The combined organic layers were dried over Na2SO4, and concentrated. The crude material was loaded onto a SCX column, washed with MeOH and diluted with 2 M NH3 in MeOH. The product-containing fractions were concentrated. Compound 3-hydroxy-4-(6-(methyl(2,2,6,6-tetramethylpiperidin-4-yl)amino)pyridazin-3-yl)-5-(trifluoromethoxy)phenyl trifluoromethanesulfonate was obtained as a yellow solid (110 mg, 28%) after flash column chromatography and HPLC purification. MS (M+1)=573.2.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08729263B2
Source datasetuspto-grants-2014_05
ORD IDord-f6c722d8137b498782a6750d822d1bf9
Source noteuspto-grants-2014_05