HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 20743Generated: October 29, 2026
Dichloroacetic Acid → HCID 11534476, compound
https://huagongshe.com/reaction/20743
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dichloroacetic Acid | HCID 6597 | — |
| Reactant | HCID 59348012 | HCID 59348012 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 11534476 | HCID 11534476 | 75% |
Reaction Steps
To (E)-5-[(2-ethylcarbamoyl-ethoxyimino)-methyl]-3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-N-(2-hydroxy-ethoxy)-benzamide (40 mg, 0.067 mmol) obtained in Step B was added dichloromethane (2 ml). The mixture was stirred at room temperature, and borane-pyridine complex (40 μl) and dichloroacetic acid (40 μl) were added thereto. After stirring for 1 hour, the reaction mixture was poured into purified water, and the resultant mixture was extracted with dichloromethane. The combined organic layers were dried over anhydrous sodium sulfate, and concentrated under reduced pressure. The residue was purified by silica gel column chromatography to give 5-[(2-ethylcarbamoyl-ethoxyamino)-methyl]-3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-N-(2-hydroxy-ethoxy)-benzamide (C-18, 29 mg, 75% yield).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07745663B2 |
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| Source dataset | uspto-grants-2010_06 |
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| ORD ID | ord-34fe0e435bf54f26b4e568ecdeeccb0d |
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| Source note | uspto-grants-2010_06 |
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