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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 545173Generated: October 29, 2026

5-Bromonicotinamide → HCID 16041930, compound

https://huagongshe.com/reaction/545173

Reaction equation

Participants

RoleNameHCIDCharge
Reactant5-BromonicotinamideHCID 1808—
Reactant1,4-DioxaneHCID 31275—
ReactantHCID 57700063HCID 57700063—
CatalystHCID 178418397HCID 178418397—
SolventChloroformHCID 6212—
ProductHCID 16041930HCID 16041930—

Reaction Steps

350 mg of 1′-[(4,8-dimethoxyquinolin-2-yl)carbonyl]-6-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)spiro[chroman-2,4′-piperidin]-4-one, 151 mg of 5-bromonicotinamide, 72.5 mg of Pd(PPh3)4 and 1.4 mL of 2M Na2CO3aq were heated with 1,4-dioxane at 100° C. and stirred for 21 hours. The reaction solution was diluted with CHCl3, filtered through Celite, and the filtrate was dried with magnesium sulfate and concentrated. The residue was purified through silica gel thin-layer chromatography (CHCl3/MeOH=9/1) to obtain the intended compound. 1H-NMR (400 MHz, CDCl3) δ: 8.90-9.00 (2H, m), 8.36 (1H, s), 8.15 (1H, s), 7.70-7.80 (2H, m), 7.40-7.55 (11H, m), 7.19 (1H, s), 7.17 (1H, d, J=8.8 Hz), 7.09 (1H, d, J=7.8 Hz), 6.3-6.5 (1H, br), 5.7-6.1 (1H, br), 4.50-4.60 (1H, m), 4.10-4.15 (1H, m), 4.08 (3H, s), 4.03 (3H, s), 3.55-3.70 (1H, m), 3.35-3.50 (1H, m), 2.88 (1H, d, J=16.6 Hz), 2.82 (1H, d, J=16.6 Hz), 2.20-2.30 (1H, m), 2.05-2.15 (1H, m), 1.80-2.05 (2H, m). MS [M+H]+=553.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07935712B2
Source datasetuspto-grants-2011_05
ORD IDord-26a4a27900dc4b0eaca5305d9632b949
Source noteuspto-grants-2011_05