HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1062286Generated: November 1, 2026
Diisopropylethylamine → HCID 10162188, compound
https://huagongshe.com/reaction/1062286
Participants
| Role | Name | HCID | Charge |
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| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | Ethanol, 2-(aminooxy)- | HCID 3014186 | — |
| Reactant | HCID 23516247 | HCID 23516247 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 10162188 | HCID 10162188 | 90% |
Reaction Steps
To a solution of 2-(2-chloro-4-iodo-phenylamino)-3,4-difluoro-benzoic acid pentafluorophenyl ester (10.0 g, 17.4 mmol) in anhydrous dimethylformamide (36 mL) was added 2-(aminooxy)-ethanol (1.6 g, 20.8 mmol) and N,N-diisopropylethylamine (6.0 mL, 34.8 mmol). The resultant solution was stirred at ambient temperature for 16 h. The reaction mixture was concentrated to 20% volume then diluted with ethyl acetate (360 mL). The resultant solution was washed with water (6×60 mL) and brine (2×60 mL). The organics were dried over anhydrous magnesium sulfate and concentrated under reduced pressure to afford a white solid that was purified on silica gel. Elution with ethyl acetate-methanol (9:1) afforded 2-(2-chloro-4-iodo-phenylamino)-3,4-difluoro-N-(2-hydroxy-ethoxy)-benzamide (7.31 g, 90%) as a white solid. Recrystallization from methanol afforded analytically pure material, identical in all respects to the material prepared by method A.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06960614B2 |
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| Source dataset | uspto-grants-2005_11 |
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| ORD ID | ord-1d2d3f985d4243fb89bb668326839f63 |
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| Source note | uspto-grants-2005_11 |
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