HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 249669Generated: October 29, 2026
4-Methylpiperidine → HCID 25128215, compound
https://huagongshe.com/reaction/249669
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4-Methylpiperidine | HCID 69381 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | Triphosgene | HCID 94429 | — |
| Reactant | HCID 178515184 | HCID 178515184 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 25128215 | HCID 25128215 | — |
Reaction Steps
A solution of 2-phenyl-2,5-dihydro-pyrazolo-(4,3-C)quinolin-3-one (4a) (0.261 g, 1 mM) in 2 mL of anhydrous methylene chloride was stirred with N,N-diisopropylethylamine (0.145 g, 1.2 mM) and triphosgene (0.173 g, 0.55 mM) at 0° C. for 1 hour and 25° C. for 2 hours. N,N-diisopropylethylamine (0.145 g, 1.2 mM) and 4-methylpiperidine (0.208 g, 2 mM) were added at 0° C. and the reaction mixture was stirred overnight at room temperature. The reaction was quenched by addition of aqueous sodium bicarbonate solution. The organic layer was collected, washed with brine solution, dried over sodium sulfate, filtered and concentrated in vacuo. The product was obtained by column chromatography. 1H NMR (CDCl3) δ (ppm): 1.0 (3H, d, J=6.59), 1.6 (4H, m), 1.84 (1H, m), 3.14 (1H, m), 3.30 (1H, m), 4.01, (1H, m), 4.60 (1H, m), 7.20 (1H, t, J=8.57), 7.38 (1H, m), 7.68-7.42 (4H, m), 8.18 (2H, m), 8.28 (1H, s), 8.44 (1H, d, J=8.81 Hz). m/z 387.5 (MH+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07863266B2 |
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| Source dataset | uspto-grants-2011_01 |
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| ORD ID | ord-9c8a46a110e3453ba08d7aee2ec3793e |
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| Source note | uspto-grants-2011_01 |
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