HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethyl orthoformate → HCID 21984054, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethyl orthoformate | HCID 31214 | — |
| Reactant | 1-(3-Amino-7-benzylquinolin-4-ylamino)-2-methylpropan-2-ol | HCID 21984192 | — |
| Reactant | 1-(3-Amino-6-benzylquinolin-4-ylamino)-2-methylpropan-2-ol | HCID 21984362 | — |
| Product | HCID 21984054 | HCID 21984054 | — |
| Product | HCID 21984293 | HCID 21984293 | — |
Reaction Steps
For Examples 431 and 434, a modification of the method described in Part B of Examples 427–429 was used to treat 1-(3-amino-7-benzylquinolin-4-ylamino)-2-methylpropan-2-ol or 1-(3-amino-6-benzylquinolin-4-ylamino)-2-methylpropan-2-ol with triethyl orthoformate, as indicated in the table below. The reaction was heated at reflux for one hour and then stirred overnight at ambient temperature. A precipitate formed, which was isolated by filtration to provide 1-(7-benzyl-1H-imidazo[4,5-c]quinolin-1-yl)-2-methylpropan-2-ol or 1-(8-benzyl-1H-imidazo[4,5-c]quinolin-1-yl)-2-methylpropan-2-ol.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07091214B2 |
| Source dataset | uspto-grants-2006_08 |
| ORD ID | ord-7c4ba5b0737a4f89b2ca5ce53f1a44b3 |
| Source note | uspto-grants-2006_08 |