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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2241999Generated: November 1, 2026

6-Chloro-m-anisidine → 5-Methoxy-8-{4-[1-(8-quinolinyl)-4-piperidinyl]-1-piperazinyl}-quinoline

https://huagongshe.com/reaction/2241999

Reaction equation

Participants

RoleNameHCIDCharge
Reactant6-Chloro-m-anisidineHCID 75460—
ReactantSodium triacetoxyborohydrideHCID 5049666—
Reactant1-Quinolin-8-yl-piperidin-4-oneHCID 59204842—
Reactant5-Methoxy-8-(piperazin-1-yl)quinolineHCID 59204862—
Product5-Methoxy-8-{4-[1-(8-quinolinyl)-4-piperidinyl]-1-piperazinyl}-quinolineHCID 12004171—

Reaction Steps

Using the synthetic methods described in previous examples, 5-methoxy-8-(piperazin-1-yl)quinoline (prepared from 2-chloro-5-methoxyaniline using the methodology described for the preparation of Example N, Step 3, above) and 1-quinolin-8-yl-piperidin-4-one (Example A, Step 5, above) were reacted with sodium triacetoxyborohydride to give the desired product as a beige solid; MP. 218-220° C.; MS (ES) m/z (relative intensity) 454 (M+H)+ (100).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07671056B2
Source datasetuspto-grants-2010_03
ORD IDord-710b00df19bf4baabe5563341ad50e24
Source noteuspto-grants-2010_03