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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 2-[4-(Benzyloxy)phenyl]cyclopropan-1-amine | HCID 43810342 | — |
| Reactant | Tert-butyl (5-(chloromethyl)-1,3,4-oxadiazol-2-yl)carbamate | HCID 86695279 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | Tert-butyl (5-(((2-(4-(benzyloxy)phenyl)cyclopropyl)amino)methyl)-1,3,4-oxadiazol-2-yl)carbamate | HCID 66715786 | 37.7% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09181198B2 |
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| Source dataset | uspto-grants-2015_11 |
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| ORD ID | ord-2d598d9143654cd397c7e6224ea62869 |
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| Source note | uspto-grants-2015_11 |
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