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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 2-(Benzhydrylideneamino)-4-bromomethylbenzonitrile | HCID 17985190 | — |
| Reactant | (S)-5-oxo-piperazine-1,3-dicarboxylic acid 1-allyl ester 3-methyl ester | HCID 53852557 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | (+/-)-4-[3-(Benzhydrylidene-amino)-4-cyano-benzyl]-5-oxo-piperazine-1,3-dicarboxylic acid 1-allyl ester 3-methyl ester | HCID 54080225 | 39% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07612075B2 |
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| Source dataset | uspto-grants-2009_11 |
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| ORD ID | ord-b0d82d1a45174ff7b1b213040136b578 |
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| Source note | uspto-grants-2009_11 |
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