HuagongsheHuagongshe Chemistry Print Report · For research reference only
6-Bromo-4-(3-chlorophenyl)-2-methoxyquinoline → [4-(3-chloro-phenyl)-2-methoxy-quinolin-6-yl]-(5-chloro-thiophen-2-yl)-(3-methyl-3H-imidazol-4-yl)-methanol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 6-Bromo-4-(3-chlorophenyl)-2-methoxyquinoline | HCID 12016672 | — |
| Reactant | (5-chloro-thiophen-2-yl)-(3-methyl-3H-imidazol-4-yl)-methanone | HCID 22465441 | — |
| Product | [4-(3-chloro-phenyl)-2-methoxy-quinolin-6-yl]-(5-chloro-thiophen-2-yl)-(3-methyl-3H-imidazol-4-yl)-methanol | HCID 22465411 | 99% |
Reaction Steps
Following the same procedure as described in example 1E, 6-bromo-4-(3-chloro-phenyl)-2-methoxy-quinoline (1.0 g, 1.87 mmol) and (5-chloro-thiophen-2-yl)-(3-methyl-3H-imidazol-4-yl)-methanone (170 mg, 3.44 mmol) generated the title compound of 18A as a yellow solid (919 mg, 65% yield).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06710209B2 |
| Source dataset | uspto-grants-2004_03 |
| ORD ID | ord-d0e336898e0e46afa7d7742aa40e7128 |
| Source note | uspto-grants-2004_03 |