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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 530362Generated: October 25, 2026

8-Chloro-1-methyl-6-(4,4,5,5-tetramethyl-[1,3,2]dioxaborolan-2-YL)-3,4-dihydro-1H-quinolin-2-one → (rac)-N-(4-(8-Chloro-1-methyl-2-oxo-1,2,3,4-tetrahydroquinolin-6-yl)-6,7-dihydro-5H-cyclopenta[c]pyridin-7-yl)propionamide

https://huagongshe.com/reaction/530362

Reaction equation

Participants

RoleNameHCIDCharge
Reactant8-Chloro-1-methyl-6-(4,4,5,5-tetramethyl-[1,3,2]dioxaborolan-2-YL)-3,4-dihydro-1H-quinolin-2-oneHCID 72208046—
ReactantN-(4-Bromo-6,7-dihydro-5H-cyclopenta[c]pyridin-7-yl)propionamideHCID 86685956—
Product(rac)-N-(4-(8-Chloro-1-methyl-2-oxo-1,2,3,4-tetrahydroquinolin-6-yl)-6,7-dihydro-5H-cyclopenta[c]pyridin-7-yl)propionamideHCID 7153846665%

Reaction Steps

In analogy to the procedure described for the preparation of example 28, 8-chloro-1-methyl-6-(4,4,5,5-tetramethyl-[1,3,2]dioxaborolan-2-yl)-3,4-dihydro-1H-quinolin-2-one (intermediate A-8) and (rac)-N-(4-bromo-6,7-dihydro-5H-cyclopenta[c]pyridin-7-yl)propionamide (intermediate A-3) were used to give the title compound as a white powder in 65% yield. MS: 384.3 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09353081B2
Source datasetuspto-grants-2016_05
ORD IDord-b6d164fdccd141ba87f5e23ec4cdd472
Source noteuspto-grants-2016_05