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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1970512Generated: November 3, 2026

(S)-4-(4-Benzyl-2H-tetrazol-5-yl)-2-tert-butoxycarbonylamino-butyric acid benzyl ester → (2S)-2-{[(tert-butoxy)carbonyl]amino}-4-(1H-1,2,3,4-tetrazol-5-yl)butanoic acid

https://huagongshe.com/reaction/1970512

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(S)-4-(4-Benzyl-2H-tetrazol-5-yl)-2-tert-butoxycarbonylamino-butyric acid benzyl esterHCID 66854446—
CatalystPalladiumHCID 23938—
SolventEthyl AcetateHCID 8857—
Product(2S)-2-{[(tert-butoxy)carbonyl]amino}-4-(1H-1,2,3,4-tetrazol-5-yl)butanoic acidHCID 66855300—

Reaction Steps

To a solution of 786 mg (S)-4-(4-benzyl-2H-tetrazol-5-yl)-2-tert-butoxycarbonylamino-butyric acid benzyl ester in 20 ml ethyl acetate was added 1.0 g Pd/C (10%) and the suspension stirred under an atmosphere of hydrogen (1 bar) for 48 h. The reaction mixture was filtrated over a plug of Celite® and washed with ethyl acetate. Yield: 516 mg colorless solid

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08426420B2
Source datasetuspto-grants-2013_04
ORD IDord-e9740fafdf0c4a7c851fcdb2c2f5ab8a
Source noteuspto-grants-2013_04