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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1433008Generated: October 31, 2026

Sodium hydride → (+/-)-4-[3-(Benzhydrylidene-amino)-4-cyano-benzyl]-5-oxo-piperazine-1,3-dicarboxylic acid 1-allyl ester 3-methyl ester

https://huagongshe.com/reaction/1433008

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium hydrideHCID 24758—
Reactant2-(Benzhydrylideneamino)-4-bromomethylbenzonitrileHCID 17985190—
Reactant(S)-5-oxo-piperazine-1,3-dicarboxylic acid 1-allyl ester 3-methyl esterHCID 53852557—
SolventDimethylformamideHCID 6228—
Product(+/-)-4-[3-(Benzhydrylidene-amino)-4-cyano-benzyl]-5-oxo-piperazine-1,3-dicarboxylic acid 1-allyl ester 3-methyl esterHCID 5408022539%

Reaction Steps

To a solution containing (S)-5-oxo-piperazine-1,3-dicarboxylic acid 1-allyl ester 3-methyl ester (0.43 g, 1.77 mmol), EXAMPLE 56, and 2-(benzhydrylidene-amino)-4-bromomethyl-benzonitrile (0.66 g, 1.77 mmol), EXAMPLE 13, in anhydrous DMF (5 mL) at 0° C. is added 60% NaH (78 mg, 1.95 mmol). After 30 min, the reaction mixture is warmed to ambient temperature and maintained for 6 hours. The reaction mixture is carefully quenched with water and then diluted with water and diethyl ether. The layers are separated and the organic phase is washed twice with water, brine, dried over anhydrous Na2SO4, filtered and concentrated. The crude residue is chromatographed on silica gel (2:1 hexane/ethyl acetate to 1:1 hexane/ethyl acetate) to provide 0.37 g (39%) of the title compound as a glassy solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07612075B2
Source datasetuspto-grants-2009_11
ORD IDord-b0d82d1a45174ff7b1b213040136b578
Source noteuspto-grants-2009_11