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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2174562Generated: October 31, 2026

Potassium bis(trimethylsilyl)amide → HCID 68352309, compound

https://huagongshe.com/reaction/2174562

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium bis(trimethylsilyl)amideHCID 3251421—
ReactantEthyl 3-methyl-1H-pyrazole-1-acetateHCID 4578874—
ReactantHCID 68352236HCID 68352236—
SolventTetrahydrofuranHCID 8028—
ProductHCID 68352309HCID 6835230973.2%

Reaction Steps

To a solution of methyl 4-amino-6-chloro-4′-(dimethylamino)-[1,1′-biphenyl]-3-carboxylate, (Intermediate 47) (416 mg, 1.365 mmol) and ethyl 2-(3-methyl-1H-pyrazol-1-yl)acetate (Alinda Chemical Ltd, 275 mg, 1.638 mmol) in THF (8.4 mL) stirred under nitrogen at room temperature was added KHMDS 1M/THF (4.09 mL, 4.09 mmol) The reaction mixture was stirred at room temperature for 20 min before being quenched with MeOH, evaporated in vacuo and taken up in water (10 mL). The aqueous layer was acidified to pH=6-7 and filtered. The precipitate obtained was washed with acetonitrile, then with diisopropyl ether and filtered to give the title compound 7-chloro-6-(4-(dimethylamino)phenyl)-4-hydroxy-3-(3-methyl-1H-pyrazol-1-yl)quinolin-2(1H)-one (415 mg, 73.2% yield) as a light yellow powder. LCMS: (M+H)+=395; Rt=2.68 min. HRMS: calculated for C21H20ClN4O2 (M+H)+: 395.1275. found: 395.1283.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09061998B2
Source datasetuspto-grants-2015_06
ORD IDord-75b762c83da74100ad9d8b0480ee6983
Source noteuspto-grants-2015_06