HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 492949Generated: October 28, 2026
HCID 23152974, compound → HCID 23153153, compound
https://huagongshe.com/reaction/492949
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | HCID 23152974 | HCID 23152974 | — |
| Reactant | 2-(4-Fluorophenyl)acetyl isocyanate | HCID 23153088 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Diisopropylethylamine | HCID 81531 | — |
| Product | HCID 23153153 | HCID 23153153 | 28% |
Reaction Steps
To a solution of 4-(4-amino-2-fluorophenoxy)-2-{[4-(2-dimethylaminoethyl)piperazin-1-yl]carbonylamino}pyridine (84.3 mg) in tetrahydrofuran (2.5 ml) were added a solution of 2-(4-fluorophenyl)acetyl isocyanate in tetrahydrofuran (0.25 M, 5.02 ml) and diisopropylethylamine (0.218 ml) at room temperature, followed by stirring overnight. The reaction mixture was partitioned between ethyl acetate and a saturated aqueous solution of sodium hydrogencarbonate. The organic layer was washed with brine and dried over anhydrous sodium sulfate. The solvent was evaporated to give a residue, which was then purified by silica gel column chromatography (Fuji Silysia NH, eluent; ethyl acetate, then ethyl acetate:methanol=95:5) to provide the titled compound (34.0 mg, 28%) as white powder.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07531532B2 |
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| Source dataset | uspto-grants-2009_05 |
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| ORD ID | ord-c7c0e4f23aca466eb8ec517518ff6ef5 |
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| Source note | uspto-grants-2009_05 |
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