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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 251710Generated: November 1, 2026

Hydroxylamine → 8-(3-((5-fluoro-2-oxoindolin-3-ylidene)methyl)benzamido)-N-hydroxyoctanamide

https://huagongshe.com/reaction/251710

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydroxylamineHCID 787—
ReactantTriethylamineHCID 8471—
ReactantEthyl chloroformateHCID 10928—
Reactant8-(3-((5-Fluoro-2-oxoindolin-3-ylidene)methyl)benzamido)octanoic acidHCID 69035705—
SolventDimethylformamideHCID 6228—
SolventSodium chloride; waterHCID 57417360—
Product8-(3-((5-fluoro-2-oxoindolin-3-ylidene)methyl)benzamido)-N-hydroxyoctanamideHCID 7660389451%

Reaction Conditions

Temperature0 °C

Reaction Steps

8-(3-((5-fluoro-2-oxoindolin-3-ylidene)methyl)benzamido)octanoic acid (424 mg, 1 mmol), triethylamine (151 mg, 1.5 mmol) and 20 ml of DMF were stirred at 0° C. while ethyl chloroformate (163 mg, 1.5 mmol) was added. The mixture was stirred at 0° C. for 2 hours, and then 50% aqueous solution of hydroxylamine (1.32 g, 20 mmol) was added. The mixture was stirred for 3 hours at room temperature, and then diluted with 1000 mL of brine. The solids were collected by vacuum filtration, washed with water and dried under vacuum to give the title compound (224 mg, 51%) as a brown solid. LC-MS (m/z) 440 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07863315B2
Source datasetuspto-grants-2011_01
ORD IDord-be4f7cc56475435783357dbd7d381b31
Source noteuspto-grants-2011_01