HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2203582Generated: October 31, 2026
Cyclohexyl isocyanate → HCID 58833613, compound
https://huagongshe.com/reaction/2203582
Participants
| Role | Name | HCID | Charge |
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| Reactant | Cyclohexyl isocyanate | HCID 18502 | — |
| Reactant | HCID 58833624 | HCID 58833624 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 58833613 | HCID 58833613 | — |
Reaction Steps
The preparation of 2-methyl-1-(2-methylpropyl)-7-(2-piperidin-4-ylethoxy)-1H-imidazo[4,5-c]quinolin-4-amine is described in Example 24. Cyclohexyl isocyanate (0.100 mL, 0.786 mmol) was added dropwise to a stirred solution of 2-methyl-1-(2-methylpropyl)-7-(2-piperidin-4-ylethoxy)-1H-imidazo[4,5-c]quinolin-4-amine (0.300 g, 0.786 mmol) in dichloromethane (10 mL) at 0° C. After 30 minutes, the solution was concentrated under reduced pressure and the resulting residue was purified by flash chromatography (silica gel, sequential elution with 2% and 5% methanol in dichloromethane) followed by recrystallization from ethanol to afford 0.141 g of 4-{2-[(4-amino-1-isobutyl-2-methyl-1H-imidazo[4,5-c]quinolin-7-yl)oxy]ethyl}-N-cyclohexylpiperidine-1-carboxamide as a white powder, mp 213.7-215.7° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09365567B2 |
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| Source dataset | uspto-grants-2016_06 |
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| ORD ID | ord-63f2379cd3d24e5b99f23cc5a61807b1 |
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| Source note | uspto-grants-2016_06 |
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