Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1047959Generated: November 4, 2026

Nitrogen → 2-[2-(2-Methyl-propenyl)-3-trifluoromethyl-benzoylamino]-indan-2-carboxylic acid ethyl ester

https://huagongshe.com/reaction/1047959

Reaction equation

Participants

RoleNameHCIDCharge
ReactantNitrogenHCID 947—
ReactantPotassium CarbonateHCID 11430—
Reactant4,4,5,5-Tetramethyl-2-(2-methylprop-1-en-1-yl)-1,3,2-dioxaborolaneHCID 15148447—
Reactant2-(2-Iodo-3-trifluoromethyl-benzoylamino)-indan-2-carboxylic acid ethyl esterHCID 59314150—
Solvent1,4-DioxaneHCID 31275—
Product2-[2-(2-Methyl-propenyl)-3-trifluoromethyl-benzoylamino]-indan-2-carboxylic acid ethyl esterHCID 68591001—

Reaction Conditions

Temperature100 °C

Reaction Steps

To a solution of 42-(2-Iodo-3-trifluoromethyl-benzoylamino)-indan-2-carboxylic acid ethyl ester (A8) (500 mg, 1.10 mmol) and 2-methyl-1-propenyl boronic acid pinacol ester (400 mg, 2.20 mmol) in dioxane (20 mL) is added dichloro[1,1′-bis(diphenylphosphino)ferrocene]-palladium (II) DCM adduct (71.8 mg, 8.2% mmol) and 2M aqueous solution of K2CO3 (1.65 mL, 3.30 mmol). The resulting reaction mixture is filled in with N2, heated to 100° C. and stirred continuously overnight. Reaction mixture is filtered and concentrated in vacuo, and the resulting residue is purified by flash column chromatography (12 g silica gel, gradient elution: 0%-50% EtOAc in heptane) to give a pure product (396) as light brown oil (100 mg, 21%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08569535B2
Source datasetuspto-grants-2013_10
ORD IDord-b3cabbe8ba3641beb622bce17f4604ea
Source noteuspto-grants-2013_10