HuagongsheHuagongshe Chemistry Print Report · For research reference only
Cyanogen Bromide → HCID 86626274, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Cyanogen Bromide | HCID 10476 | — |
| Reactant | 2-Chloro-N~4~-(2-methylpropyl)quinoline-3,4-diamine | HCID 11747039 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 86626274 | HCID 86626274 | — |
Reaction Steps
A solution of 2-chloro-N4-(2-methylpropyl)-3,4-quinolinediamine (André et al, U.S. Pat. No. 4,988,815, Example 6, 8.92 g, 35.7 mmol) in ethanol (50 mL) was stirred at 100° C.; cyanogen bromide (5.67 g, 53.5 mmol) was added in one portion. The red solution was stirred overnight, washed three times with water, and washed once with brine. A precipitate formed in the aqueous washings and was isolated by filtration. The organic fraction was dried over magnesium sulfate, filtered through a layer of CELITE filer agent, concentrated under reduced pressure, further dried under high vacuum, and combined with the isolated precipitate to provide 9.81 g of 4-chloro-1-(2-methylpropyl)-1H-imidazo[4,5-c]quinoline-2-amine hydrobromide as a dark red solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08143270B2 |
| Source dataset | uspto-grants-2012_03 |
| ORD ID | ord-a198fe4280b4467b9588fb7e93c36643 |
| Source note | uspto-grants-2012_03 |