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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantDiisopropylethylamineHCID 81531—
Reactant4-AminotetrahydropyranHCID 419223—
Reactant6-Bromo-4-chloro-3-quinolinecarboxamideHCID 67514264—
SolventDimethylacetamideHCID 31374—
Product6-Bromo-4-(oxan-4-ylamino)quinoline-3-carboxamideHCID 11849879593.3%

Reaction Conditions

Temperature90 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09428503B2
Source datasetuspto-grants-2016_08
ORD IDord-53287217a7dd4957959eb757c4ce78bf
Source noteuspto-grants-2016_08