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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2371158Generated: November 4, 2026

Sodium Hydroxide → tert-butyl (2S)-2-[(4-{[(3,4-dichlorophenyl)amino]-carbonyl}piperazin-1-yl)methyl]morpholine-4-carboxylate

https://huagongshe.com/reaction/2371158

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium HydroxideHCID 14798—
ReactantSodium ThiosulfateHCID 24477—
ReactantDiisopropylethylamineHCID 81531—
ReactantTriacetoxyperiodinaneHCID 159087—
Reactant(R)-N-Boc-2-hydroxymethylmorpholineHCID 1512576—
ReactantSodium triacetoxyborohydrideHCID 5049666—
ReactantN-(3,4-dichlorophenyl)piperazine-1-carboxamide hydrochlorideHCID 46743200—
SolventDichloromethaneHCID 6344—
Producttert-butyl (2S)-2-[(4-{[(3,4-dichlorophenyl)amino]-carbonyl}piperazin-1-yl)methyl]morpholine-4-carboxylateHCID 5765685324.1%

Reaction Steps

Dess-Martin periodinane (8.60 g) was added to tert-butyl (2R)-2-(hydroxymethyl)morpholine-4-carboxylate (4.00 g) in dry DCM at 0° C. The reaction was warmed to RT and stirred for a further 2 h. Aqueous sodium thiosulfate (10% w/v, 50 ml) was added and the DCM layer was removed then dried (MgSO4), filtered and evaporated to form the crude aldehyde. The residue was then dissolved in dry dichloromethane (100 ml) followed by addition of N-(3,4-dichlorophenyl)piperazine-1-carboxamide hydrochloride (5.72 g), N, N-diisopropylethylamine (3.17 mL) and NaBH(OAc)3 (9.76 g) and the reaction was stirred under argon for 18 h. 1M NaOH (50 mL) was added followed by vigorous stirring and the dichloromethane layer was extracted. The organic layer was dried (MgSO4), filtered and evaporated. Purification by chromatography (EtOAc neat) afforded the title compound (2.10 g) as a white foam.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08710224B2
Source datasetuspto-grants-2014_04
ORD IDord-0528fbe1ee724e589af00e0ed62e119d
Source noteuspto-grants-2014_04