HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1802487Generated: November 1, 2026
2-Chloro-4,6-difluoroaniline → HCID 59436014, compound
https://huagongshe.com/reaction/1802487
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2-Chloro-4,6-difluoroaniline | HCID 2734083 | — |
| Reactant | Sodium t-butoxide | HCID 23676156 | — |
| Reactant | HCID 59436091 | HCID 59436091 | — |
| Reactant | HCID 59436097 | HCID 59436097 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 59436014 | HCID 59436014 | — |
| Product | HCID 59436106 | HCID 59436106 | — |
Reaction Steps
To a solution of 1.5:1 mixture of 6-chloro-10-ethoxypyrido[4,3-c]-1,6-naphthyridine and 6,10-dichloropyrido[4,3-c]-1,6-naphthyridine (1.5 g) in THF (25 mL) was added 2-chloro-4,6 difluoro aniline (945 mg, 5.78 mmol) and sodium tert-butoxide (1.65 g, 17 mmol). The solution was heated to 85° C. for 40 min then cooled to room temperature and extracted with EtOAc and brine. The organic layers were dried with MgSO4, filtered, and concentrated under reduced pressure. The crude residue was purified on silica gel (100% hexanes to 100% EtOAc, gradient elution) which provided N-(2-chloro-4,6-difluorophenyl)-10-ethoxypyrido[4,3-c]-1,6-naphthyridin-6-amine and 10-chloro-N-(2-chloro-4,6-difluorophenyl)pyrido[4,3-c]-1,6-naphthyridin-6-amine.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08349865B2 |
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| Source dataset | uspto-grants-2013_01 |
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| ORD ID | ord-d4a4e8bfa27e41ac9cc1803335175697 |
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| Source note | uspto-grants-2013_01 |
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