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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1774791Generated: November 1, 2026

3,5-Dibromopyridine → HCID 137329756, compound

https://huagongshe.com/reaction/1774791

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3,5-DibromopyridineHCID 69369—
ReactantHCID 131734728HCID 131734728—
ProductHCID 137329756HCID 137329756—

Reaction Steps

In analogy to the procedures described for the preparation of intermediate A-3 [B] and A-3 [C]: i) (R)-1-(tert-butyl-dimethyl-silanyloxymethyl)-2-methyl-propylamine has been reacted with 3,5-dibromopyridine to give (5-bromo-pyridin-3-yl)-[(R)-1-(tert-butyl-dimethyl-silanyloxymethyl)-2-methyl-propyl]-amine; ii) subsequent condensation with 1-methyl-6-(4,4,5,5-tetramethyl-[1,3,2]dioxaborolan-2-yl)-3,4-dihydro-1H-quinolin-2-one (intermediate A-1) gave the title compound as light yellow amorphous solid. MS: 454.3 (M+H+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09260408B2
Source datasetuspto-grants-2016_02
ORD IDord-d2338681d9024b50a597dd8b56d16017
Source noteuspto-grants-2016_02