HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2084013Generated: October 31, 2026
4-Chloro-6,7-dimethoxyquinoline → HCID 22732274, compound
https://huagongshe.com/reaction/2084013
Participants
| Role | Name | HCID | Charge |
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| Reactant | 4-Chloro-6,7-dimethoxyquinoline | HCID 459610 | — |
| Reactant | HCID 22057981 | HCID 22057981 | — |
| Solvent | Isopropanol | HCID 3776 | — |
| Product | HCID 22732274 | HCID 22732274 | — |
Reaction Steps
4-Chloro-6,7-dimethoxyquinoline (WO 98/13350 A1) (150 mg) and N-(3-amino-4-methylphenyl)-3-dimethylaminobenzamide (199 mg) were stirred in isopropanol (5 ml) and heated to 85° C. for 18 hours. After cooling to room temperature the precipitated solid was isolated and washed with isohexane. Filtered solid was impure and so was purified by eluting through a silica column with 10% methanol in methylene chloride. The title compound was obtained as a solid (35 mg); NMR: 2.14 (s, 3H), 2.94 (s, 6H), 3.89 (s, 3H), 3.93 (s, 3H), 6.05 (m, 1H), 6.90 (m, 1H), 7.18 (m, 1H), 7.22 (m, 1H), 7.3 (m, 1H), 7.61 (m, 1H), 7.73 (s, 1H), 7.78 (m, 1H), 8.18 (d, 1H), 8.47 (s, 1H), 10.1 (s, 1H); m/s: M+H+ 457.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06716847B2 |
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| Source dataset | uspto-grants-2004_04 |
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| ORD ID | ord-c456246741d742ff8c5a6700c00eed75 |
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| Source note | uspto-grants-2004_04 |
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