HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 501970Generated: October 30, 2026
1,4'-Bipiperidine → HCID 59424297, compound
https://huagongshe.com/reaction/501970
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1,4'-Bipiperidine | HCID 78607 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | HCID 59424353 | HCID 59424353 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 59424297 | HCID 59424297 | 96% |
Reaction Steps
(R)-2-(4-(8-Fluoro-2-oxo-1,2-dihydroquinolin-3-yl)piperidine-1-carbonyloxy)-3-(7-methyl-2-((2-(trimethylsilyl)ethoxy)methyl)-2H-indazol-5-yl)propanoic acid (105 mg, 0.17 mmol) was dissolved in N,N-dimethylformamide (3 mL). N,N-Diisopropylethylamine (100 μL, 0.57 mmol) was added to the mixture followed by o-benzotriazol-1-yl-N,N,N′-tetramethyluronium tetrafluoroborate (65 mg, 0.20 mmol). The reaction was stirred at room temperature for 5 min. 4-Piperidinopiperidine (41 mg, 0.22 mmol) was added to the mixture. The reaction was stirred at room temperature for 2 h. The mixture was diluted with ethyl acetae (25 mL), washed successively with water (3×), and brine. The organic layer was dried (magnesium sulfate), filtered, and concentrated in vacuo. The title compound was obtained without further purification as white solid in 96% yield. Mass spec.: 773.3 (MH)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07772244B2 |
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| Source dataset | uspto-grants-2010_08 |
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| ORD ID | ord-aa204a1168d541f5b1a03f42b343bd4f |
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| Source note | uspto-grants-2010_08 |
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