HuagongsheHuagongshe Chemistry Print Report · For research reference only
Quinoline → HCID 178498500, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Quinoline | HCID 7047 | — |
| Reactant | 2-(Methylthio)aniline | HCID 76337 | — |
| Reactant | HCID 178498511 | HCID 178498511 | — |
| Product | HCID 178498500 | HCID 178498500 | 59% |
Reaction Steps
Employing the same sequence as employed in the preparation of quinoline F3 but starting with the commercially available o-toluidene (Aldrich Chemical Co.) rather than 2-methylmercaptoaniline (F1) the desired quinoline I1 was obtained (1.24 g, 59% yield over two steps).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07642235B2 |
| Source dataset | uspto-grants-2010_01 |
| ORD ID | ord-b7b282921ffd4fd6892c7431aea042c0 |
| Source note | uspto-grants-2010_01 |