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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 717079Generated: October 30, 2026

HCID 14901692, compound → HCID 71735151, compound

https://huagongshe.com/reaction/717079

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 14901692HCID 14901692—
ReactantHCID 16895372HCID 16895372—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
ProductHCID 71735151HCID 7173515113.7%

Reaction Conditions

Temperature-78 °C

Reaction Steps

3-Chloro-N,N-diethyl-2-methyl-benzamide (150 mg, 0.66 mmol) was dissolved in anhydrous THF (2 mL) under N2 and cooled to −78° C. n-BuLi (2.5M in n-hexanes, 558 μL, 1.39 mmol) was added dropwise and the reaction mixture was stirred at −78° C. for 30 minutes. 4-Cyano-N-(1-methyl-piperidin-4-ylmethyl)-benzamide (180 mg, 0.66 mmol) in anhydrous THF (2 mL) was added dropwise to the reaction mixture and stirred at −78° C. continued for 1 h. The reaction mixture was poured into ice/water, allowed to warm to RT and extracted with CH2Cl2 (×3) and the organic phase dried (MgSO4). The solution was filtered and concentrated in vacuo. The crude material was purified by reverse phase preparative HPLC-MS to afford 4-(5-chloro-1-oxo-1,2-dihydro-isoquinolin-3-yl)-N-(1-methyl-piperidin-4-ylmethyl)-benzamide as a white solid (37 mg, 13%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09193689B2
Source datasetuspto-grants-2015_11
ORD IDord-cf924d25813e4e2da0a4834f9aca1324
Source noteuspto-grants-2015_11