HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 533720Generated: October 29, 2026
2-Methylpiperidine → HCID 24981321, compound
https://huagongshe.com/reaction/533720
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2-Methylpiperidine | HCID 7974 | — |
| Reactant | Carbonate Ion | HCID 19660 | — |
| Reactant | 1-Hydroxybenzotriazole | HCID 75771 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | Carbodiimide | HCID 160435 | — |
| Reactant | HCID 12092493 | HCID 12092493 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 24981321 | HCID 24981321 | 383.5% |
Reaction Steps
To a solution of 4-(4-fluorophenylcarbamoyl)benzoic acid (50 mg, 0.19 mmol) in DMF (1 mL) was added PS-Carbodiimide (125 mg, 0.25 mmol), HOBt (26 mg, 0.19 mmol), DIPEA (52 mg, 0.40 mmol) and 2-methylpiperidine (25 mg, 0.25 mmol). The reaction was agitated at room temperature for 18 h. To the reaction was added MP-carbonate and agitated for a further 8 h. The reaction was filtered and concentrated under vacuum to afford diluted with water (10 mL) and isolated the white precipitate by vacuum filtration to afford N-(4-fluorophenyl)-4-(2-methylpiperidine-1-carbonyl)benzamide (248 mg, 95%). 1H-nmr (400 MHz, d6-DMSO) δ 10.37 (br s, 1H), 8.00 (d, J=7 Hz, 2H), 7.83-7.72 (m, 2H), 7.49 (d, J=7 Hz, 2H), 7.21 (t, J=8 Hz, 2H), 3.52-3.01 (m, 3H), 1.75-1.29 (m, 6H), 1.21 (m, 3H); MS (ESI) m/z 341.4.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08853392B2 |
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| Source dataset | uspto-grants-2014_10 |
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| ORD ID | ord-da1b2751822b4a2d96c878ddb891e75c |
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| Source note | uspto-grants-2014_10 |
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