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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1972796Generated: November 2, 2026

Sodium Carbonate → HCID 131730545, compound

https://huagongshe.com/reaction/1972796

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium CarbonateHCID 10340—
ReactantTriphenylphosphineHCID 11776—
Reactant2-benzyl-6-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-2H-IndazoleHCID 58529313—
ReactantHCID 131730546HCID 131730546—
Catalystpalladium(II) acetateHCID 167845—
SolventTolueneHCID 1140—
Solvent1,4-DioxaneHCID 31275—
ProductHCID 131730545HCID 13173054566%

Reaction Conditions

Temperature90 °C

Reaction Steps

Pd(OAc)2 (11 mg, 0.05 mmol) was suspended in a degassed mixture of 3:2 toluene:dioxane and PPh3 (52 mg, 0.20 mmol) was added. The mixture was stirred for 10 minutes and then the product from step 3 (433 mg, 1.00 mmol) and Intermediate C (434 mg, 1.30 mmol) were added followed by 2.5 mL of 2M aqueous Na2CO3 solution. The mixture was heated to 90° C. overnight. The reaction was allowed to cool to rt and partitioned between water and EtOAc. The layers were separated and the aqueous layer was extracted with EtOAc. The combined organic phases were washed with brine, dried (Na2SO4), filtered and concentrated in vacuo. The residue was purified by Isco® (Redi-sep 40, eluting with 75-100% EtOAc/Hexanes) to provide 368 mg (66%) of the title compound as an off-white solid. 1H-NMR (DMSO-d6) 8.44 (s, 1H), 7.98 (s, 1H), 7.84 (s, 1H), 7.82 (m, 1H), 7.74 (d, 1H), 7.56 (s, 1H), 7.50-7.39 (m, 2H), 7.31 (t, 1H), 7.26-7.12 (m, 5H), 7.08 (d, 1H), 7.00, (s, 1H), 5.57 (s, 2H), 4.64 (s, 2H) 0.82 (s, 9H), 0.01 (s, 6H); LC-MS [M+H]+=561.5, RT=3.65 min.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08431695B2
Source datasetuspto-grants-2013_04
ORD IDord-b883d89023264d90b9e650bc5f35db4f
Source noteuspto-grants-2013_04