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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 530357Generated: October 27, 2026

Sodium Carbonate → (rac)-N-[4-(7-Fluoro-1-methyl-2-oxo-1,2,3,4-tetrahydro-quinolin-6-yl)-5,6,7,8-tetrahydro isoquinolin-8-yl]-propionamide

https://huagongshe.com/reaction/530357

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium CarbonateHCID 10340—
ReactantHCID 86679131HCID 86679131—
ReactantN-(4-Bromo-5,6,7,8-tetrahydroisoquinolin-8-yl)propionamideHCID 86685953—
SolventDimethylformamideHCID 6228—
Product(rac)-N-[4-(7-Fluoro-1-methyl-2-oxo-1,2,3,4-tetrahydro-quinolin-6-yl)-5,6,7,8-tetrahydro isoquinolin-8-yl]-propionamideHCID 7153704663%

Reaction Conditions

Temperature100 °C

Reaction Steps

A mixture of 7-fluoro-1-methyl-6-(4,4,5,5-tetramethyl-[1,3,2]dioxaborolan-2-yl)-3,4-dihydro-1H-quinolin-2-one (intermediate A-9, 168 mg, 0.55 mmol) and (rac)-N-(4-bromo-5,6,7,8-tetrahydro-isoquinolin-8-yl)-propionamide (intermediate B-1) (142 mg, 0.5 mmol) in DMF (3 mL) was purged with argon for 1 min before bis(triphenylphosphine)palladium (II)chloride (38 mg, 0.054 mmol) and 1 N aq. Na2CO3 (2.5 mL) were added. The resulting reaction mixture was purged with argon for 2 min, and heated at 100° C. for 45 min in a microwave. After cooling to room temperature, the reaction mixture was diluted with EtOAc (5 mL) before it was poured into a satd. aq. solution of NaHCO3 (10 mL). The aqueous layer was extracted with EtOAc (3×5 mL) and the combined organic layers were washed with water and brine, dried over anhy. Na2SO4, filtered and concentrated in vacuo. The residue was purified by prep-HPLC to give the title compound (120 mg, 63% yield) as a white solid. MS: 382.3 (M+H)+

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09353081B2
Source datasetuspto-grants-2016_05
ORD IDord-2a4895b82a9f4dfcbc664cbe3e9fe1ff
Source noteuspto-grants-2016_05