HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-Chloro-6,7-dimethoxy-quinoline-3-carbonitrile → 4-(6-Chloro-4-iodo-2,3-methylenedioxyan ilino)-3-cyano-6,7-dimethoxyquinoline
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-Chloro-6,7-dimethoxy-quinoline-3-carbonitrile | HCID 10586676 | — |
| Reactant | 5-Chloro-7-iodo-1,3-benzodioxol-4-amine | HCID 17980527 | — |
| Product | 4-(6-Chloro-4-iodo-2,3-methylenedioxyan ilino)-3-cyano-6,7-dimethoxyquinoline | HCID 17980510 | 72.6% |
Reaction Steps
Using an analogous procedure to that described in the portion of Example 1 that is concerned with the preparation of starting materials, 4-chloro-3-cyano-6,7-dimethoxyquinoline (1.74 g) was reacted with 6-chloro-4-iodo-2,3-methylenedioxyaniline (2.5 g) to give 4-(6-chloro-4-iodo-2,3-methylenedioxyanilino)-3-cyano-6,7-dimethoxyquinoline as a solid (2.59 g) which gave the following characterising data; NMR Spectrum: (DMSOd6) 4.0 (s, 6H), 6.18 (s, 2H), 7.38 (s, 1H), 7.48 (s, 1H), 7.88 (s, 1H), 8.44 (s, 1H), 9.45 (s, 1H); Mass Spectrum: M+H+ 510.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07173135B2 |
| Source dataset | uspto-grants-2007_02 |
| ORD ID | ord-9b2e43c34ee24c14b92906835591507e |
| Source note | uspto-grants-2007_02 |