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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2407681Generated: November 1, 2026

Binap, (A+-)- → HCID 58504049, compound

https://huagongshe.com/reaction/2407681

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBinap, (A+-)-HCID 634876—
ReactantHCID 22479811HCID 22479811—
ReactantSodium t-butoxideHCID 23676156—
ReactantHCID 58504252HCID 58504252—
SolventTolueneHCID 1140—
ProductHCID 58504049HCID 58504049—

Reaction Conditions

Temperature100 °C

Reaction Steps

3-Bromo-1-(tetrahydro-2H-pyran-2-yl)-5-(1-trityl-1H-1,2,4-triazol-3-yl)-1H-indazole (0.25 g, prepared according to the reported preparation in US 2004/0127536), the compound prepared in Example 9 (0.29 g), racemic-2,2′-bis(diphenylphosphino)-1,1′-binaphthyl (0.040 g), and sodium tert-butoxide (0.20 g) were suspended in toluene (6 mL) and purged with argon. Tris(dibenzylideneacetone)dipalladium(0) (0.019 g) was added and the system was sealed and heated at 100° C. overnight. The reaction mixture was cooled to room temperature and partitioned between dichloromethane and a saturated aqueous sodium bicarbonate solution. The organics were dried over anhydrous magnesium sulfate and concentrated. The residue was purified by column chromatography on silica gel to obtain the title compound (0.13 g) having the following physical data.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08809538B2
Source datasetuspto-grants-2014_08
ORD IDord-3fa005591d3f45e2b2170897c04c9218
Source noteuspto-grants-2014_08