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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 472528Generated: October 30, 2026

1,2,3,4-Tetrahydroquinoline → HCID 59612418, compound

https://huagongshe.com/reaction/472528

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,2,3,4-TetrahydroquinolineHCID 69460—
Reactant8-Bromo-2-chloro-[1,2,4]triazolo[1,5-a]pyridineHCID 67481370—
ProductHCID 59612418HCID 59612418—

Reaction Steps

1,1′-[1,2,4]triazolo[1,5-a]pyridine-2,5-diyldi-1,2,3,4-tetrahydroquinoline was prepared from 8-bromo-2-chloro-[1,2,4]triazolo[1,5-a]pyridine (500.0 mg, 2.15 mmol) and 1,2,3,4-tetrahydro-quinoline (274.0 mg, 2.04 mmol) in a manner analogous to Example 2d. Byproduct was isolated as a brown solid (0.033 g, 4%). 1H NMR (400 MHz, CDCl3, δ, ppm): 8.14 (d, J=8.2 Hz, 1H), 7.40-7.35 (m, 1H), 7.32-7.28 (m, 1H), 7.15-7.05 (m, 3H), 6.98 (t, J=7.5 Hz, 1H), 6.91-6.84 (m, 2H), 6.69-6.62 (m, 2H), 4.09-4.05 (m, 2H), 3.88-3.83 (m, 2H), 2.93 (t, J=6.4 Hz, 2H), 2.82 (t, J=6.4 Hz, 2H), 2.10-1.80 (m, 4H). MS=382 (MH)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08633173B2
Source datasetuspto-grants-2014_01
ORD IDord-693741abb409464aa61cea9919bab76c
Source noteuspto-grants-2014_01