Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Benzenesulfonyl chloride, 2,4-dichloro- | HCID 204419 | — |
| Reactant | 5-Chloro-6-(quinolin-3-yloxy)pyridin-3-amine | HCID 68790798 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 24853027 | HCID 24853027 | — |
Reaction Steps
Dry dichloromethane (15 mL) was added to 5-Chloro-6-(quinolin-3-yloxy)-pyridin-3-yl amine (250 mg, 1 mmol) obtained in preparation 1. To the stirred solution was added 2,4-dichlorobenzenesulfonyl chloride (492 mg, 2.2 mmol) followed by the addition of triethylamine (2.2 mmol). The reaction mixture was then maintained at 45° C. for 15 hours, cooled to room temperature (25° C.) and diluted with dichloromethane. The dichloromethane layer was washed with water, dried over sodium sulfate and concentrated under vacuum to get the crude, which was further purified by column chromatography (silica gel).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08269010B2 |
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| Source dataset | uspto-grants-2012_09 |
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| ORD ID | ord-298b7e01ef58444a9d30c9ce6bd0e53c |
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| Source note | uspto-grants-2012_09 |
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