HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 888017Generated: October 27, 2026
Acetic Anhydride → HCID 68408763, compound
https://huagongshe.com/reaction/888017
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | N-(2-Aminophenyl)-4-piperidin-4-ylbenzamide | HCID 16225584 | — |
| Solvent | Dimethylacetamide | HCID 31374 | — |
| Product | HCID 68408763 | HCID 68408763 | 68.2% |
Reaction Steps
N-(2-aminophenyl)-4-piperidin-4-ylbenzamide (Example 5, 30 mg, 0.10 mmol) was stirred and dissolved in N,N-dimethylacetamide (2 ml) and acetic anhydride (0.011 ml, 0.11 mmol) added. The reaction was stirred at ambient temperature for 1 hour and then partitioned between water and ethyl acetate. The organic layer was separated, washed with brine and dried over magnesium sulfate, filtered and evaporated to give the title compound as a colourless solid (23 mg, 68%); NMR Spectrum: (DMSO-d6) 1.48 (m, 1H), 1.64 (m, 1H), 1.79 (m, 2H), 2.02 (s, 3H), 2.59 (m, 1H), 2.84 (m, 1H), 3.13 (m, 1H), 3.92 (d, 1H), 4.53 (d, 1H), 4.85 (s, 2H), 6.58 (m, 1H), 6.76 (d, 1H), 6.95 (m, 1H), 7.15 (d, 1H), 7.37 (d, 2H), 7.90 (d, 2H), 9.55 (s, 1H); Mass Spectrum: M+H+ 338.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08247562B2 |
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| Source dataset | uspto-grants-2012_08 |
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| ORD ID | ord-acd2004a7f414ae59a7f45fe7a22be70 |
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| Source note | uspto-grants-2012_08 |
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