HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1836402Generated: October 30, 2026
Phenyl isocyanate → 4-[3-(Phenylureido)benzoyl]-1-methylpiperidine
https://huagongshe.com/reaction/1836402
Participants
| Role | Name | HCID | Charge |
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| Reactant | Phenyl isocyanate | HCID 7672 | — |
| Reactant | 4-[3-Aminobenzoyl]-1-methylpiperidine | HCID 10130651 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 4-[3-(Phenylureido)benzoyl]-1-methylpiperidine | HCID 23499329 | 74% |
Reaction Steps
4-[3-aminobenzoyl]-1-methylpiperidine (25 mg, 0.115 mmol) and phenyl isocyanate (37 μL, 0.344 mmol) in methylene chloride (2 mL) were mixed for 72 h at ambient temperature. The solution was diluted with 10% acetic acid in methanol and poured over a Varian Mega Bond Elut™ strong cation exchange column. The column was rinsed extensively with methanol to remove impurities, then treated with a 2M ammonia in methanol to elute the product from the column. The solvent was evaporated and the residue was stirred with 5N sodium hydroxide solution (1 mL). The solvent was removed under vacuum and the residue was purified by silica gel chromatography (methylene chloride:methanol:ammonium hydroxide, 97.5:2.5:0.25 then 95:5:0.5). The solvent was evaporated to give 28.5 mg (74%) of the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06777428B1 |
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| Source dataset | uspto-grants-2004_08 |
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| ORD ID | ord-e6247230952442b8916308b1af3aa6b6 |
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| Source note | uspto-grants-2004_08 |
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