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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 79081Generated: October 29, 2026

1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimide → 7-(2-Fluoro-4-iodo-phenylamino)-benzo[d]isothiazole-6-carboxylic acid (2-vinyloxy-ethoxy)-amide

https://huagongshe.com/reaction/79081

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimideHCID 15908—
Reactant1-HydroxybenzotriazoleHCID 75771—
ReactantDiisopropylethylamineHCID 81531—
ReactantO-(2-(Vinyloxy)ethyl)hydroxylamineHCID 21867017—
Reactant7-(2-Fluoro-4-iodo-phenylamino)-benzo[d]isothiazole-6-carboxylic acidHCID 57521504—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
Product7-(2-Fluoro-4-iodo-phenylamino)-benzo[d]isothiazole-6-carboxylic acid (2-vinyloxy-ethoxy)-amideHCID 5752150649.2%

Reaction Steps

To a solution of 7-(2-fluoro-4-iodo-phenylamino)-benzo[d]isothiazole-6-carboxylic acid (328 mg, 0.79 mmol) and diisopropylethylamine (0.41 mL, 2.37 mmol) in DMF (2 mL) were added O-(2-vinyloxy-ethyl)-hydroxylamine (163 mg, 1.58 mmol), EDCI (303 mg, 1.58 mmol) and HOBt (213 mg, 1.58 mmol). The reaction mixture was stirred for 18 hours at room temperature, diluted with ethyl acetate, and washed with water then a saturated aqueous solution of sodium hydrogen carbonate, then brine, before being dried (Na2SO4), filtered and concentrated in vacuo. The resultant residue was subjected to flash chromatography (Si—PPC, gradient 0% to 100%, TBME in cyclohexane) to afford the title compound as a yellow foam (194 mg, 49%). LCMS (method B): RT=3.99 min, [M+H]+=500.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08841462B2
Source datasetuspto-grants-2014_09
ORD IDord-5b079de4d51c49f482d757b2d6dfc764
Source noteuspto-grants-2014_09