HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 661266Generated: October 25, 2026
Ethanol → (3-{3-[Cyclopropyl(methyl)amino]-1,2,4-oxadiazol-5-yl}-5-[4-(trifluoromethyl)phenyl]piperidin-1-yl)(morpholin-4-yl)methanone
https://huagongshe.com/reaction/661266
Participants
| Role | Name | HCID | Charge |
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| Reactant | Ethanol | HCID 702 | — |
| Reactant | Cyclopropanemethanamine | HCID 75646 | — |
| Reactant | {3-(3-Chloro-1,2,4-oxadiazol-5-yl)-5-[4-(trifluoromethyl)phenyl]piperidin-1-yl}(morpholin-4-yl)methanone | HCID 58116540 | — |
| Product | (3-{3-[Cyclopropyl(methyl)amino]-1,2,4-oxadiazol-5-yl}-5-[4-(trifluoromethyl)phenyl]piperidin-1-yl)(morpholin-4-yl)methanone | HCID 49819151 | — |
Reaction Steps
To a solution of 109 mg (0.245 mmol) of the oxadiazole from Example 23A in 2.0 ml of ethanol were added 523 mg (7.35 mmol) of cyclopropylmethylamine, and then the reaction mixture was stirred in the microwave at 90° C. for 12 h. The solvent was removed under reduced pressure and the crude product was purified by means of preparative HPLC. Yield: 42.0 mg (36% of theory)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08084469B2 |
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| Source dataset | uspto-grants-2011_12 |
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| ORD ID | ord-214eb9ad2b2c4edfa21a8ce7efedf63f |
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| Source note | uspto-grants-2011_12 |
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