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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1627563Generated: October 31, 2026

Sodium hydride → HCID 54579457, compound

https://huagongshe.com/reaction/1627563

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium hydrideHCID 24758—
Reactant4-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrazoleHCID 2774010—
Reactanttert-Butyl 1-oxa-6-azaspiro(2.5)octane-6-carboxylateHCID 22135564—
SolventDimethylformamideHCID 6228—
ProductHCID 54579457HCID 5457945789%

Reaction Conditions

Temperature90 °C

Reaction Steps

A reaction mixture of compound (3-2) (214 mg; 1.0 mmol) and 4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrazole (3-3, 194 mg; 1.0 mmol) with NaH 60% dispersion in mineral oil (60 mg; 1.5 mmol) in 3 mL of DMF was stirred at 90° C. for 3 hours. The reaction mixture was partitioned between EtOAc (200 mL) and saturated NaHCO3 solution (50 mL) and brine (50 mL). The organic layer was dried (Na2SO4) and concentrated by vacuum to give 361 mg of (3-4) as a yellow grease (89% yield). 1H NMR (400 MHz, chloroform-D) δ ppm 1.21-1.34 (m, 12H) 1.39-1.50 (m, 9H) 1.56-1.78 (m, 4H) 3.14 (s, 2H) 3.72-3.91 (m, J=32.34 Hz, 2H) 4.05 (s, 2H) 7.65 (s, 1H) 7.80 (s, 1H) 8.00 (s, 1H). LCMS calcd for C20H34BN3O5 (M+H) 408, found 408. HPLC purity 85%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08785632B2
Source datasetuspto-grants-2014_07
ORD IDord-e4125927cac94443b74a7cbf99fe6f92
Source noteuspto-grants-2014_07