HuagongsheHuagongshe Chemistry Print Report · For research reference only
Isobutylamine → HCID 57545324, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Isobutylamine | HCID 6558 | — |
| Reactant | Propylamine | HCID 7852 | — |
| Reactant | Fluorobenzene | HCID 10008 | — |
| Reactant | 1-Fluoro-4-(methylsulphonyl)benzene | HCID 67994 | — |
| Reactant | 1,1,1-Trimethoxybutane | HCID 123512 | — |
| Reactant | 3-Methoxypropanoyl chloride | HCID 2759728 | — |
| Reactant | HCID 67050950 | HCID 67050950 | — |
| Product | HCID 57545324 | HCID 57545324 | — |
Reaction Steps
The general methods described in Parts A-G of Example 1 were used to prepare 7-benzyloxy-2-(2-methoxyethyl)-1-propyl-1H-imidazo[4,5-c]quinoline. Propylamine was used in lieu of isobutylamine in Part E, and methoxypropionyl chloride was used in lieu of trimethyl orthobutyrate in Part G. 7-Benzyloxy-2-(2-methoxyethyl)-1H-propyl-1H-imidazo[4,5-c]quinoline was treated according to the general methods described in Parts A-D of Examples 35-40. In Part B, the fluorobenzene used was 4-fluorophenyl methyl sulfone. Following chromatographic purification, the product was recrystallized from acetonitrile to provide 0.890 g of 7-(4-methanesulfonylphenoxy)-2-(2-methoxyethyl)-1-propyl-1H-imidazo[4,5-c]quinolin-4-amine as dark tan needles, mp 210-212° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07897597B2 |
| Source dataset | uspto-grants-2011_03 |
| ORD ID | ord-959129b2984d4dc6a99602b3fff2708f |
| Source note | uspto-grants-2011_03 |