HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 545173Generated: October 29, 2026
5-Bromonicotinamide → HCID 16041930, compound
https://huagongshe.com/reaction/545173
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 5-Bromonicotinamide | HCID 1808 | — |
| Reactant | 1,4-Dioxane | HCID 31275 | — |
| Reactant | HCID 57700063 | HCID 57700063 | — |
| Catalyst | HCID 178418397 | HCID 178418397 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | HCID 16041930 | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07935712B2 |
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| Source dataset | uspto-grants-2011_05 |
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| ORD ID | ord-26a4a27900dc4b0eaca5305d9632b949 |
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| Source note | uspto-grants-2011_05 |
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