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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 708355Generated: October 29, 2026

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

https://huagongshe.com/reaction/708355

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl ((2R,3S)-2-((5-methyl-2H-tetrazol-2-yl)methyl)-4-oxoazetidin-3-yl)carbamateHCID 131733725—
CatalystPalladiumHCID 23938—
SolventEthylacetate methanolHCID 21584119—
Product(3S,4R)-3-amino-4-((5-methyl-2H-tetrazol-2-yl)methyl)azetidin-2-oneHCID 118379665—

Reaction Steps

Prepared in an analogous manner to example 4, step 3 using benzyl ((2R,3S)-2-((5-methyl-2H-tetrazol-2-yl)methyl)-4-oxoazetidin-3-yl)carbamate (111 mg, 0.351 mmol) and Pd on C (10%, 50 mg) in EtOAc:MeOH (5:1, 7.0 mL) for 3 h. The crude residue was used as such in following step. LCMS: Rt=0.14 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-d7d260bc71b54709a661895aa4f10822
Source noteuspto-grants-2015_11