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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 708359Generated: October 29, 2026

Benzyl ((2R,3S)-2-((5-methyl-1H-tetrazol-1-yl)methyl)-4-oxoazetidin-3-yl)carbamate → (3S,4R)-3-amino-4-((5-methyl-1H-tetrazol-1-yl)methyl)azetidin-2-one

https://huagongshe.com/reaction/708359

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl ((2R,3S)-2-((5-methyl-1H-tetrazol-1-yl)methyl)-4-oxoazetidin-3-yl)carbamateHCID 131733728—
CatalystPalladiumHCID 23938—
SolventEthanol, mixt. with methanolHCID 18681192—
Product(3S,4R)-3-amino-4-((5-methyl-1H-tetrazol-1-yl)methyl)azetidin-2-oneHCID 118379653—

Reaction Steps

Prepared in an analogous manner to example 4, step 3 using benzyl ((2R,3S)-2-((5-methyl-1H-tetrazol-1-yl)methyl)-4-oxoazetidin-3-yl)carbamate (97 mg, 0.31 mmol) and Pd on C (10%, 50 mg) in EtOH:MeOH (5:1, 3.0 mL) for 3 h. The crude residue was used as such in following step. LCMS: Rt=0.11 min, m/z=183.2 (M+1) Method 2m_acidic.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09174978B2
Source datasetuspto-grants-2015_11
ORD IDord-54a50fd8445c40fdb720e111d70ca18c
Source noteuspto-grants-2015_11