HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1836407Generated: November 1, 2026
Isopropyl isocyanate → HCID 23499364, compound
https://huagongshe.com/reaction/1836407
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Isopropyl isocyanate | HCID 61277 | — |
| Reactant | 4-[3-Aminobenzoyl]-1-methylpiperidine | HCID 10130651 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 23499364 | HCID 23499364 | 63% |
Reaction Steps
4-[3-aminobenzoyl]-1-methylpiperidine (25 mg, 0.115 mmol) and poly(4-vinyl pyridine) (50 mg, 0.400 mmol, 2% cross-linked) in tetrahydrofuran (2 mL) were allowed to stand 10 min. Isopropyl isocyanate (34 μL, 0.344 mmol) was added and the reaction mixture was mixed for 96 h at ambient temperature. The reaction mixture was filtered and the filter cake was rinsed with methanol. Glacial acetic acid (0.5 mL) was added to the filtrate solution and the solution was mixed. This mixture was 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 purified by silica gel chromatography (1-3% gradient, 2M ammonia in methanol:methylene chloride). The solvent was evaporated to give 21.8 mg (63%) 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-07f0e0e5db19447886b1e29504845110 |
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| Source note | uspto-grants-2004_08 |
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