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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1394443Generated: October 25, 2026

1-Heptanethiol → 4-[1-Phenyl-1-(5-(azetidin-3-yl)-1,3,4-oxadiazol-2-yl)methylene]piperidine-1-carboxylic acid tert-butyl ester

https://huagongshe.com/reaction/1394443

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-HeptanethiolHCID 15422—
Reactant4-[1-Phenyl-1-(5-(N-(9-fluorenylmethoxycarbonyl)azetidin-3-yl)-1,3,4-oxadiazol-2-yl)methylene]piperidine-1-carboxylic acid tert-butyl esterHCID 67046374—
Catalyst1,8-Diazabicyclo(5.4.0)undec-7-eneHCID 81184—
SolventTetrahydrofuranHCID 8028—
Product4-[1-Phenyl-1-(5-(azetidin-3-yl)-1,3,4-oxadiazol-2-yl)methylene]piperidine-1-carboxylic acid tert-butyl esterHCID 6704644174.7%

Reaction Steps

To a solution of 4-[1-phenyl-1-(5-(N-(9-fluorenylmethoxycarbonyl)azetidin-3-yl)-1,3,4-oxadiazol-2-yl)methylene]piperidine-1-carboxylic acid tert-butyl ester(0.161 g, 0.260 mmol) and heptanethiol (0.398 mL, 2.60 mmol) in THF (2.6 mL) at rt was added DBU (2 drops). The mixture was allowed to stir for 18 h and then the solvent was removed in vacuo. The residue was dissolved in MeOH and purified by preparative HPLC (NH4OAc) to afford the title compound (0.077 g, 74%) as a colorless solid:

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07348337B2
Source datasetuspto-grants-2008_03
ORD IDord-2d607c958dfb4d49b25aa88e082ffc3b
Source noteuspto-grants-2008_03