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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 712695Generated: October 26, 2026

1-(3-Bromo-5-chloro-pyridin-4-yl)-ethanol → 1-[3-Chloro-5-(5,6,7,8-tetrahydro-[1,8]naphthyridin-3-yl)-pyridin-4-yl]-ethanol

https://huagongshe.com/reaction/712695

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-(3-Bromo-5-chloro-pyridin-4-yl)-ethanolHCID 67155021—
Reactant6-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)-1,2,3,4-tetrahydro-1,8-naphthyridineHCID 118989928—
Product1-[3-Chloro-5-(5,6,7,8-tetrahydro-[1,8]naphthyridin-3-yl)-pyridin-4-yl]-ethanolHCID 117667165—

Reaction Steps

1-[3-Chloro-5-(5,6,7,8-tetrahydro-[1,8]naphthyridin-3-yl)-pyridin-4-yl]-ethanol is synthesized according to the procedure of Suzuki Coupling Method VI using 1-(3-bromo-5-chloro-pyridin-4-yl)-ethanol (which is prepared according to Step 1 of Example 78) and crude 6-(4,4,5,5-tetramethyl-[1,3,2]dioxaborolan-2-yl)-1,2,3,4-tetrahydro-[1,8]naphthyridine (that is prepared according to Step 4 of Example 105).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09181272B2
Source datasetuspto-grants-2015_11
ORD IDord-f89eab1dfed046478776f80b4ebfc44d
Source noteuspto-grants-2015_11