HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 598271Generated: October 29, 2026
HCID 67050910, compound → HCID 57545338, compound
https://huagongshe.com/reaction/598271
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | HCID 67050910 | HCID 67050910 | — |
| Reactant | HCID 67050947 | HCID 67050947 | — |
| Product | HCID 57545338 | HCID 57545338 | — |
Reaction Steps
A modification of the general method described in Example 41 was followed using 1-(2-methylpropyl)-7-(2-nitrophenoxy)-2-propyl-1H-imidazo[4,5-c]quinolin-4-amine, prepared as described in Example 36, in lieu of 1-(2-methylpropyl)-7-(4-nitrophenoxy)-2-propyl-1H-imidazo[4,5-c]quinolin-4-amine. When the reaction was complete, the reaction mixture was filtered through a layer of CELITE filter aid, and the filter cake was washed with methanol and methanol:dichloromethane. Following treatment with the ion exchange resin, the crude product was purified by column chromatography on silica gel (eluting with dichloromethane:methanol ranging in ratios from 98:2 to 94:6). The white, waxy solid was recrystallized from acetonitrile to yield 0.150 g of 7-(2-aminophenoxy)-1-(2-methylpropyl)-2-propyl-1H-imidazo[4,5-c]quinolin-4-amine as tan crystals, mp 197-199° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07897597B2 |
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| Source dataset | uspto-grants-2011_03 |
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| ORD ID | ord-dbf170f9a3b54f0b9d0968b5c7ed7f24 |
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| Source note | uspto-grants-2011_03 |
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