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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 709419Generated: October 31, 2026

Potassium Carbonate → Tert-butyl (5-(((2-(4-(benzyloxy)phenyl)cyclopropyl)amino)methyl)-1,3,4-oxadiazol-2-yl)carbamate

https://huagongshe.com/reaction/709419

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant2-[4-(Benzyloxy)phenyl]cyclopropan-1-amineHCID 43810342—
ReactantTert-butyl (5-(chloromethyl)-1,3,4-oxadiazol-2-yl)carbamateHCID 86695279—
SolventDimethylformamideHCID 6228—
ProductTert-butyl (5-(((2-(4-(benzyloxy)phenyl)cyclopropyl)amino)methyl)-1,3,4-oxadiazol-2-yl)carbamateHCID 6671578637.7%

Reaction Steps

Tert-butyl (5-(chloromethyl)-1,3,4-oxadiazol-2-yl)carbamate (141 mg, 0.606 mmol) was added to a solution of 2-(4-(benzyloxy)phenyl)cyclopropanamine (enantiomer (−)) (145 mg, 0.606 mmol) and K2CO3 (166 mg, 1.213 mmol) in dry DMF (1.5 mL) and stirred at RT for 2 h. After completion, the reaction mixture was poured into ice water (10 mL) and extracted with EtOAc (4×10 mL). The combined organic extracts were washed with water (3×10 mL), brine (10 mL), dried over anhydrous Na2SO4, filtered and concentrated under vacuum. The residue obtained was purified by column chromatography (SiO2) using MeOH:CHCl3 (1:99) as eluent to afford tert-butyl (5-(((2-(4-(benzyloxy)phenyl)cyclopropyl)amino)methyl)-1,3,4-oxadiazol-2-yl)carbamate (enantiomer-(−)) (100 mg, 37.7%) as a pale green liquid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09181198B2
Source datasetuspto-grants-2015_11
ORD IDord-2d598d9143654cd397c7e6224ea62869
Source noteuspto-grants-2015_11