HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 405028Generated: October 30, 2026
4-Methylpiperidine → HCID 58032534, compound
https://huagongshe.com/reaction/405028
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4-Methylpiperidine | HCID 69381 | — |
| Reactant | HCID 66630755 | HCID 66630755 | — |
| Reactant | HCID 66631055 | HCID 66631055 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 58032534 | HCID 58032534 | 71.4% |
Reaction Steps
3-{3-Fluoro-4-[5-(4-methyl-piperidine-1-carbonyl)-[1,2,4]oxadiazol-3-yl]-phenyl}-2-[(4′-methyl-biphenyl-3-carbonyl)-amino]-propionic acid tert-butyl ester. A mixture of 3-(4-{2-tert-butoxycarbonyl-2-[(4′-methyl-biphenyl-3-carbonyl)-amino]-ethyl}-2-fluoro-phenyl)-[1,2,4]oxadiazole-5-carboxylic acid methyl ester (50 mg) and 4-methyl-piperidine (13.5 mg) in MeOH (3 mL) was heated at 55° C. for 25 min in a microwave reactor. TLC showed the reaction was completed. The mixture was concentrated, 10 mL of 1N aq. HCl solution and 20 mL of ethyl acetate were added. The layers were separated and the aqueous portion was extracted with ethyl acetate (2×10 mL). The combined organic layers were washed with brine (2×30 mL), dried over anhydrous sodium sulfate, filtered, and concentrated to give the title compound (40 mg, 71.4% yield).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08748412B2 |
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| Source dataset | uspto-grants-2014_06 |
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| ORD ID | ord-717fcc39c1b84e02a34d6153fd6cdf6a |
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| Source note | uspto-grants-2014_06 |
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