HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1070513Generated: October 28, 2026
Sodium Bicarbonate → N-[1-(4-Chloro-3-fluorobenzyl)-4-piperidinyl]-3-[3-(2-pyridinyl)-1,2,4-oxadiazol-5-yl]propanamide
https://huagongshe.com/reaction/1070513
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | 3-(3-pyridin-2-yl-1,2,4-oxadiazol-5-yl)propanoic acid | HCID 3164328 | — |
| Reactant | 1-(4-Chloro-3-fluorobenzyl)-4-piperidinamine | HCID 22396205 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | N-[1-(4-Chloro-3-fluorobenzyl)-4-piperidinyl]-3-[3-(2-pyridinyl)-1,2,4-oxadiazol-5-yl]propanamide | HCID 22396154 | — |
Reaction Steps
3-[3-(2-Pyridinyl)-1,2,4-oxadiazol-5-yl]propanoic acid (0.136 g) and N,N′-carbonyldiimidazole (0.114 g) were stirred in dichloromethane (10 ml) under nitrogen for 1 hour. 1-(4-Chloro-3-fluorobenzyl)-4-piperidinamine (0.150 g) was then added and left to stir for 2 hours. Saturated sodium hydrogen carbonate was added to the reaction, with the resulting solution being extracted three times with dichloromethane. The pooled organic phases were washed once with water, once with brine, dried over magnesium sulfate, filtered and the solvent removed under reduced pressure to leave an oil. This was triturated with diethyl ether which caused product the to crystallise. After filtration, the product was washed with diethyl ether and dried to N-[1-(4-chloro-3-fluorobenzyl)-4-piperidinyl]-3-[3-(2-pyridinyl)-1,2,4-oxadiazol-5-yl]propanamide. m.p. 132° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06903085B1 |
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| Source dataset | uspto-grants-2005_06 |
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| ORD ID | ord-58379b9279144aaeacbf622b872cb3d4 |
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| Source note | uspto-grants-2005_06 |
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