HuagongsheHuagongshe Chemistry Print Report · For research reference only
Thionyl Chloride → HCID 67052428, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | HCID 10149351 | HCID 10149351 | — |
| Solvent | 1,2-Dichloroethane | HCID 11 | — |
| Product | HCID 67052428 | HCID 67052428 | — |
Reaction Steps
Thionyl chloride (2.65 mL, 36.2 mmol) was added dropwise to a stirred suspension of [4-amino-1-(2-methylpropyl)-6,7,8,9-tetrahydro-1H-imidazo[4,5-c]quinolin-2-yl]methanol (4.97 g, 18.1 mmol) in 1,2-dichloroethane (200 mL). The suspension dissolved, then a precipitate formed after 5 minutes. The reaction mixture was stirred at room temperature for 6 hours, then was concentrated under reduced pressure to yield crude 2-(chloromethyl)-1-(2-methylpropyl)-6,7,8,9-tetrahydro-1H-imidazo[4,5-c]quinolin-4-amine hydrochloride, all of which was used in the next step.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07897767B2 |
| Source dataset | uspto-grants-2011_03 |
| ORD ID | ord-94fa83fcaf204321ae733c5cba3e64d7 |
| Source note | uspto-grants-2011_03 |