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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 730661Generated: October 29, 2026

Tetrahydrofuran → HCID 136335820, compound

https://huagongshe.com/reaction/730661

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
ReactantHCID 136335821HCID 136335821—
ReactantHCID 178418361HCID 178418361—
CatalystPalladiumHCID 23938—
SolventDichloromethaneHCID 6344—
ProductHCID 136335820HCID 136335820—

Reaction Steps

A solution of 2.50 g (4.38 mmol) (R)-2-(4-benzyloxy-3,5-dimethyl-phenyl)-1-carboxy-ethyl 4-(5-oxo-3-phenyl-4,5-dihydro-1,2,4-triazol-1-yl)-piperidine-1-carboxylate in 50 mL DCM was combined with 250 mg 10% Pd/C and hydrogenated at RT and 3 bar hydrogen pressure for 4.5 h. To complete the reaction a further 250 mg of catalyst were added, the mixture was hydrogenated for 12 h at 40° C., combined with 25 mL THF and 250 mg catalyst and hydrogenated for a further 12 h at 40° C. The catalyst was removed by suction filtering and the filtrate was concentrated by evaporation i. vac. The residue was stirred with DIPE, suction filtered and dried.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07582625B2
Source datasetuspto-grants-2009_09
ORD IDord-00e80ecf9d0a4e268bf53b1c98976a74
Source noteuspto-grants-2009_09