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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 21338Generated: October 30, 2026

Water → HCID 86628337, compound

https://huagongshe.com/reaction/21338

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantDimethylformamideHCID 6228—
ReactantLDA THF ethylbenzene heptaneHCID 86590273—
Reactant2-bromo-N-(1-methyl-1-phenylethyl)nicotinamideHCID 86628336—
SolventTetrahydrofuranHCID 8028—
ProductHCID 86628337HCID 8662833725.3%

Reaction Steps

2-Bromo-N-(1-methyl-1-phenylethyl)nicotinamide (500 mg, 1.57 mmol) was dissolved in THF (20 mL), and the solution was added with LDA-heptane/THF/ethylbenzene solution (2.0 mol/L, 3.5 mL, 7.1 mmol) by drops at −78° C. for 25 minutes under argon atmosphere, followed by stirring at the same temperature for 1.6 hours. Then, the mixture was added with DMF (0.267 mL, 3.45 mmol) and warmed from −78° C. to room temperature over 1 hour. The reaction mixture was added with water and extracted with ethyl acetate. The organic layer was washed with saturated brine and dried over anhydrous sodium sulfate. The solvent was evaporated under reduced pressure and the residue was purified by flash column chromatography (chloroform/methanol=100/1 to 97/3) to obtain 4-bromo-1-hydroxy-2-(1-methyl-1-phenylethyl)-1,2-dihydropyrrolo[3,4-c]pyridine-3-one (138 mg, yield 25%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07745641B2
Source datasetuspto-grants-2010_06
ORD IDord-cda688a316bd420eb4294ebce63fa3f3
Source noteuspto-grants-2010_06