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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1264483Generated: October 28, 2026

HCID 59049327, compound → HCID 59049307, compound

https://huagongshe.com/reaction/1264483

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 59049327HCID 59049327—
CatalystPalladiumHCID 23938—
SolventEthanolHCID 702—
ProductHCID 59049307HCID 59049307—

Reaction Steps

(2S)-1-(Benzyloxycarbonyl)-2-(1-[3-(3-pyridyl)-1-propyl]-1H-tetrazol-5-yl)azetidine from Reference Example 17 (125.3 mg, 0.331 mmol, 1.0 eq) was dissolved in ethanol (20 mL) and 10% Pd/C (49.9 mg, 0.047 mmol, 0.14 eq) was carefully added. The mixture was flushed with vacuum and nitrogen three times and stirred under a hydrogen atmosphere at about room temperature for about 26 hours. After removing the solid matter by filtration, the solvent was removed under vacuum to give 80.8 mg (quantitative yield) of the product as a colorless oil. 1H NMR (CDCl3) δ 2.18-3.24 (series of m, 7H); 3.46-4.68 (series of m, 5H); 7.19-7.33 (m, 1H); 7.51-7.63 (m, 1H); 8.38-8.57 (m, 2H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06544976B1
Source datasetuspto-grants-2003_04
ORD IDord-019a7228a3f648b8b893780e04b9c643
Source noteuspto-grants-2003_04