HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1371313Generated: October 28, 2026
1-(4-aminobutyl)-2-(2-methoxyethyl)-1H-imidazo[4,5-c]quinolin-4-amine → HCID 22344444, compound
https://huagongshe.com/reaction/1371313
Participants
| Role | Name | HCID | Charge |
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| Reactant | 1-(4-aminobutyl)-2-(2-methoxyethyl)-1H-imidazo[4,5-c]quinolin-4-amine | HCID 22180872 | — |
| Catalyst | Adams' catalyst | HCID 345198 | — |
| Solvent | Trifluoroacetic acid | HCID 6422 | — |
| Product | HCID 22344444 | HCID 22344444 | 45% |
Reaction Steps
A catalytic amount of platinum (IV) oxide was added to a solution of 1-(4-aminobutyl)-2-methoxyethyl-1H-imidazo[4,5-c]quinolin-4-amine (7.7 g, 24.5 mmol) in trifluoroacetic acid (250 mL). The reaction mixture was hydrogenated at 50 psi (3.44×105 Pa) on a Parr apparatus. The progress of the reaction was monitored by LC/MS. Additional catalyst was added 7, 11, and 17 days after the start of the reaction. After 25 days the reaction was complete. The reaction mixture was filtered through a layer of Celite® filter aid to remove the catalyst and the filtrate was concentrated under vacuum. The residue was combined with 1 N hydrochloric acid (100 mL) and stirred overnight. The mixture was made basic (pH=11) with ammonium hydroxide and then extracted with dichloromethane (3×300 mL). The extracts were combined and concentrated under vacuum to provide 3.5 g of 1-(4-aminobutyl)-6,7,8,9-tetrahydro-2-methoxyethyl-1H-imidazo[4,5-c]quinolin-4-amine as a solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07157453B2 |
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| Source dataset | uspto-grants-2007_01 |
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| ORD ID | ord-9658d6a90f86407f95c5705328ec7acc |
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| Source note | uspto-grants-2007_01 |
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