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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1062330Generated: November 2, 2026

HCID 69611306, compound → HCID 69611293, compound

https://huagongshe.com/reaction/1062330

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 69611306HCID 69611306—
ReactantHCID 178418361HCID 178418361—
CatalystPalladiumHCID 23938—
SolventMethanolHCID 887—
ProductHCID 69611293HCID 69611293—

Reaction Steps

A solution of crude tert-butyl 2-((2S,3S)-3-{[(benzyloxy)carbonyl]-amino}-2-hydroxy-4-(3,5-difluorophenyl)butyl)-2-ethylhydrazinecarboxylate (906 mg, 1.8 mmol) in MeOH (15 mL) was added to 10% Pd/C (95 mg) and stirred in a hydrogen atmosphere (ambient pressure) for 4 h. The catalyst was filtered off over Celite and the filtrate was concentrated under reduced pressure to yield crude tert-butyl 2-((2S, 3S)-3-amino-2-hydroxy-4-(3,5difluorophenyl)butyl)-2-ethylhydrazinecarboxylate. MS (ESI+) for C17H27F2N3O3 m/z 360.2 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06960664B2
Source datasetuspto-grants-2005_11
ORD IDord-5be4fcf78cdb40f8bd1d4fe1db33e73d
Source noteuspto-grants-2005_11