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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 20743Generated: October 29, 2026

Dichloroacetic Acid → HCID 11534476, compound

https://huagongshe.com/reaction/20743

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDichloroacetic AcidHCID 6597—
ReactantHCID 59348012HCID 59348012—
SolventDichloromethaneHCID 6344—
ProductHCID 11534476HCID 1153447675%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07745663B2
Source datasetuspto-grants-2010_06
ORD IDord-34fe0e435bf54f26b4e568ecdeeccb0d
Source noteuspto-grants-2010_06