HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2265649Generated: October 30, 2026
HCID 23152981, compound → HCID 59596927, compound
https://huagongshe.com/reaction/2265649
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | HCID 23152981 | HCID 23152981 | — |
| Reactant | [4-(3-fluoro-4-{[1-(4-fluorophenylcarbamoyl)cyclopropanecarbonyl]amino}phenoxy)pyridin-2-yl]-N-(phenoxycarbonyl)carbamic acid phenyl ester | HCID 59597026 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 59596927 | HCID 59596927 | 65.9% |
Reaction Steps
To a solution of phenyl N-[4-(3-fluoro-4-{[1-(4-fluorophenylcarbamoyl)cyclopropanecarbonyl]amino}phenoxy)pyridin-2-yl]-N-phenoxycarbonylcarbamate (50.0 mg) in N,N-dimethylformamide (2.0 ml) was added N-[1-(2-dimethylaminoethyl)piperidin-4-yl]-N-methylamine (69.5 mg), followed by stirring at room temperature for 22 hr. The reaction mixture was partitioned between ethyl acetate and a 1N aqueous solution of sodium hydroxide. The organic layer was washed with brine, and dried over anhydrous sodium sulfate. The solvent was removed, and the residue was purified by silica gel column chromatography (Fuji Silysia NH, ethyl acetate, then ethyl acetate:methanol=20:1). Fractions containing the target compound were concentrated. To the residue was added diethyl ether:hexane=1:3, and the precipitate was collected by filtration. This was washed with hexane and dried under aeration to provide the titled compound as white powder (31.4 mg, 65.9%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07855290B2 |
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| Source dataset | uspto-grants-2010_12 |
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| ORD ID | ord-0c3d5759eb364f1bb562de8a7e647d28 |
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| Source note | uspto-grants-2010_12 |
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