HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1486922Generated: October 30, 2026
Water → 6-Bromo-4-(oxan-4-ylamino)quinoline-3-carboxamide
https://huagongshe.com/reaction/1486922
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | 4-Aminotetrahydropyran | HCID 419223 | — |
| Reactant | 6-Bromo-4-chloro-3-quinolinecarboxamide | HCID 67514264 | — |
| Solvent | Dimethylacetamide | HCID 31374 | — |
| Product | 6-Bromo-4-(oxan-4-ylamino)quinoline-3-carboxamide | HCID 118498795 | 93.3% |
Reaction Steps
A mixture of 6-bromo-4-chloroquinoline-3-carboxamide (50 g, 175.4 mmol), tetrahydro-2H-pyran-4-amine (26.2 g, 193 mmol) and DIPEA (56.13 mL, 438.5 mmol) in DMA (500 mL) was stirred at 90° C. overnight. The mixture was allowed to cool and poured into water (1500 mL). The precipitate was filtered, washed with water (2×200 mL) and dried under reduced pressure to afford the desired material (57.3 g, 93%) as a white solid. NMR Spectrum: 1H NMR (400 MHz, DMSO-d6) δ 2.88-1.92 (2H, m), 2.59-2.78 (2H, m), 3.50-3.62 (3H, m), 3.96-4.08 (2H, m), 4.92-4.98 (1H, m), 7.80 (1H, m), 7.99 (1H, dd), 8.46 (1H, d), 8.74 (1H, s).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09428503B2 |
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| Source dataset | uspto-grants-2016_08 |
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| ORD ID | ord-53287217a7dd4957959eb757c4ce78bf |
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| Source note | uspto-grants-2016_08 |
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