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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 216656Generated: October 29, 2026

Potassium Carbonate → 5-(Tert-butyl-diphenyl-silanyloxymethyl)-2-methyl-pyrazolo[1,5-a]pyridine

https://huagongshe.com/reaction/216656

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
ReactantO-(2,4,6-Trimethylbenzenesulfonyl)hydroxylamineHCID 11830845—
Reactant4-(Tert-butyl-diphenyl-silanyloxymethyl)-2-prop-1-ynyl-pyridineHCID 131729750—
SolventWaterHCID 962—
SolventChloroformHCID 6212—
Product5-(Tert-butyl-diphenyl-silanyloxymethyl)-2-methyl-pyrazolo[1,5-a]pyridineHCID 13172974942%

Reaction Steps

A solution of O-mesitylenesulfonylhydroxylamine (18.6 g, 77.8 mmol, 5.0 equiv) in chloroform (50 ml) is added at 0-10° C. to a solution of 4-(tert-butyl-diphenyl-silanyloxymethyl)-2-prop-1-ynyl-pyridine in chloroform (50 ml). The resulting mixture is stirred at room temperature overnight. The solvent is removed in vacuo, and N,N-dimethylformamide (50 ml) is added to the residue. Potassium carbonate (4.30 g, 31.1 mmol, 2.0 equiv) is added, and the mixture is stirred at room temperature for 2 hours. The reaction mixture is diluted with water and extracted three times with EtOAc. The combined organic layers are washed with brine, dried over Na2SO4, filtered and concentrated in vacuo. Purification via flash chromatography (gradient from hexane/EtOAc 100:0 to 30:70) affords the title compound (2.6 g, 42%). 1H NMR (400 MHz, d6-DMSO): δ=8.42 (d, J=7.1 Hz, 1H), 7.60-7.58 (m, 4H), 7.43-7.35 (m, 7H), 6.64 (dd, J=7.3/1.9 Hz, 1H), 6.27 (s, 1H), 4.71 (s, 2H), 2.30 (s, 3H), 0.99 (s, 9H). MS (ES+): 401 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08193236B2
Source datasetuspto-grants-2012_06
ORD IDord-4d488241359f4e8a9e4a035a4674cae1
Source noteuspto-grants-2012_06