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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1404772Generated: October 26, 2026

Sulfuric Acid → 6-((5-chloro-3H-[1,2,3]triazolo[4,5-b]pyridin-3-yl)methyl)quinoline

https://huagongshe.com/reaction/1404772

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSulfuric AcidHCID 1118—
ReactantSodium BicarbonateHCID 516892—
ReactantSodium NitriteHCID 23668193—
Reactant6-chloro-N2-(quinolin-6-ylmethyl)pyridine-2,3-diamineHCID 86698078—
SolventAcetic AcidHCID 176—
SolventWaterHCID 962—
Product6-((5-chloro-3H-[1,2,3]triazolo[4,5-b]pyridin-3-yl)methyl)quinolineHCID 5851460196.4%

Reaction Conditions

Temperature5 °C

Reaction Steps

Intermediate 9 (0.220 g, 0.772 mmol) was dissolved in acetic acid (1.3 ml) and cooled to 5° C. Sodium nitrite (0.063 g, 0.927 mmol) in 0.35 ml water was added slowly followed by sulphuric acid (0.09 ml). The reaction mixture was warmed to RT and stirred for 30 mm. The reaction mixture was poured into ice water and pH adjusted to ca. 8 with sodium bicarbonate solution, extracted with ethyl acetate, washed with brine, dried over sodium sulphate and concentrated to afford the title compound as a brown solid (0.220 g. 96%). 1H-NMR (δ ppm, DMSO-d6, 400 MHz): δ8.88 (s, 1H), 8.69 (d, J=8.6 Hz, 1H), 8.35 (d, J=8.1 Hz, 1H), 8.01 (d, J=8.6 Hz, 1H), 7.90 (s, 1H), 7.74 (d, J=8.5 Hz, 1H), 7.61 (d, J=8.5 Hz. 1H), 7.53 (dd, J=8.0, 4.0 Hz, 1H), 6.12 (s, 2H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08912331B2
Source datasetuspto-grants-2014_12
ORD IDord-abc6d5ec4cbb4b72859a90c8909e875c
Source noteuspto-grants-2014_12