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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 539720Generated: October 26, 2026

(R)-benzyl 2-methylpiperazine-1-carboxylate → (R)-benzyl 4-(3-amino-2-fluorobenzyl)-2-methylpiperazine-1-carboxylate

https://huagongshe.com/reaction/539720

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(R)-benzyl 2-methylpiperazine-1-carboxylateHCID 40424346—
Reactant3-Amino-2-fluorobenzaldehydeHCID 55282197—
SolventTetrahydrofuranHCID 8028—
Product(R)-benzyl 4-(3-amino-2-fluorobenzyl)-2-methylpiperazine-1-carboxylateHCID 58919233108.8%

Reaction Steps

To a room temperature solution of (R)-benzyl 2-methylpiperazine-1-carboxylate (1.7 g, 7.2 mmol, 1.0 equiv) and 3-amino-2-fluorobenzaldehyde (1.0 g, 7.2 mmol, 1.0 equiv) in THF (10 mL) was added NaHB(OAc)3 (3.84 g, 18.1 mmol, 2.5 equiv) as a solid in one portion. After stirring at room temperature for 1.5 h, the reaction was complete, as determined by LCMS. The remaining reducing reagent was quenched by the careful addition of aq. satd. NaHCO3, and the mixture was diluted with EtOAc. The layers were separated and the organic layer was washed with aq. satd. NaHCO3 and brine, dried over sodium sulfate and concentrated in vacuo to provide (R)-benzyl 4-(3-amino-2-fluorobenzyl)-2-methylpiperazine-1-carboxylate (2.8 g, >100% mass recovery). The material was used without further purification. LCMS m/z (APCI)=358.5 (M+H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08871768B2
Source datasetuspto-grants-2014_10
ORD IDord-f337ae41161f404ab11a9c13d2009ced
Source noteuspto-grants-2014_10