HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 746504Generated: October 26, 2026
Toluene → N1-[5-(2-methyl-1H-imidazo[4,5-c]quinolin-1-yl)pentyl]benzamide
https://huagongshe.com/reaction/746504
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Toluene | HCID 1140 | — |
| Reactant | Triethylorthoaceate | HCID 21875354 | — |
| Reactant | N-{5-[(3-nitroquinolin-4-yl)amino]pentyl}benzamide | HCID 23512735 | — |
| Catalyst | Platinum | HCID 23939 | — |
| Solvent | Isopropanol | HCID 3776 | — |
| Product | N1-[5-(2-methyl-1H-imidazo[4,5-c]quinolin-1-yl)pentyl]benzamide | HCID 23512678 | — |
Reaction Steps
A catalytic amount of platinum on carbon was added to a suspension of N1-{5-[(3-nitroquinolin-4-yl)amino]pentyl}benzamide (3.4 g, 9 mmol) in isopropyl alcohol (250 mL). The reaction mixture was placed under a hydrogen atmosphere at 50 psi (3.4×104 pascals) on a Parr apparatus. After 2 hours the reaction mixture was filtered to remove the catalyst. The filtrate was concentrated under vacuum to provide crude N1-{5-[(3-aminoquinolin-4-yl)amino]pentyl}benzamide. This material was combined with triethylorthoacetate (1.4 g, 9 mmol) and toluene (200 mL). The reaction mixture was heated overnight on a steam bath with a Vigreux column. The toluene was decanted from the reaction mixture and concentrated under vacuum to provide N1-[5-(2-methyl-1H-imidazo[4,5-c]quinolin-1-yl)pentyl]benzamide as an oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07393859B2 |
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| Source dataset | uspto-grants-2008_07 |
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| ORD ID | ord-1677026e3234415caf7b4be9627abfa2 |
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| Source note | uspto-grants-2008_07 |
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