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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1873355Generated: November 1, 2026

Triphenylphosphine → HCID 42635877, compound

https://huagongshe.com/reaction/1873355

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriphenylphosphineHCID 11776—
Reactant2-((4-Methylbenzenesulfonyl)oxy)ethan-1-olHCID 249155—
ReactantDiisopropyl azodicarboxylateHCID 5363146—
ReactantHCID 24864014HCID 24864014—
SolventChloroformHCID 6212—
SolventDimethylformamideHCID 6228—
ProductHCID 42635877HCID 4263587712.2%

Reaction Steps

To 10 mL of a solution of 639 mg (corresponding to 2.95 mmol) of 2-hydroxyethyl-p-toluenesulfonate in tetrahydrofran, 388 mg (corresponding to 1.34 mmol) of 6-bromo-2-(4′-hydroxyphenyl)imidazo[1,2-a]pyridine and 780 mg (corresponding to 2.97 mmol) of triphenylphosphine were added. Further, 6 mL of N,N-dimethylformamide was added thereto to completely dissolve the contents. To the reaction mixture, 0.58 mL (corresponding to 2.95 mmol) of diisopropylazodicarboxylate was added. After the reaction mixture was stirred at room temperature for 17 hours, the reaction solution was concentrated. The resulting crude product was purified by flash silica gel column chromatography (elution solvent: hexane/ethyl acetate=65/35). Insoluble matter in chloroform was filtered out of fractions containing a target compound. Further, the resulting crude product was purified by recycle preparative HPLC (HPLC apparatus: LC-908 (under trade name; manufactured by Japan Analytical Industry Co., Ltd.); column: two JAIGEL 2H (under trade name; manufactured by Japan Analytical Industry Co., Ltd.) connected together; mobile phase: chloroform), to obtain 79.7 mg (corresponding to 164 μmol) of 6-bromo-2-[4′-(2″-p-toluenesulfonyloxyethoxy)phenyl]imidazo[1,2-a]pyridine (FIG. 1-3, Step 4).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08303935B2
Source datasetuspto-grants-2012_11
ORD IDord-ce964345e486457e971f719b553cf7d8
Source noteuspto-grants-2012_11