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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 708377Generated: October 30, 2026

Benzyl ((2R,3S)-2-((1H-1,2,4-triazol-1-yl)methyl)-4-oxoazetidin-3-yl)carbamate → (3S,4R)-4-((1H-1,2,4-triazol-1-yl)methyl)-3-aminoazetidin-2-one

https://huagongshe.com/reaction/708377

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl ((2R,3S)-2-((1H-1,2,4-triazol-1-yl)methyl)-4-oxoazetidin-3-yl)carbamateHCID 131733730—
CatalystPalladiumHCID 23938—
SolventEthanol, mixt. with methanolHCID 18681192—
Product(3S,4R)-4-((1H-1,2,4-triazol-1-yl)methyl)-3-aminoazetidin-2-oneHCID 118390218—

Reaction Steps

Prepared in an analogous manner to example 4, step 3 using benzyl ((2R,3S)-2-((1H-1,2,4-triazol-1-yl)methyl)-4-oxoazetidin-3-yl)carbamate (250 mg, 0.830 mmol) and Pd on C (10%, 125 mg) in EtOH:MeOH (4:1, 8.3 mL) for 3 h. The crude residue was used as such in following step. LCMS: Rt=0.13 min, m/z=168.1 (M+1) Method 2m_acidic.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09174978B2
Source datasetuspto-grants-2015_11
ORD IDord-e0ccdae725bf46bea5460486373827b6
Source noteuspto-grants-2015_11