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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1047749Generated: October 29, 2026

Diisopropylethylamine → 5-Fluoro-2-(2-isopropoxy-3-methyl-benzoylamino)-indan-2-carboxylic acid ethyl ester

https://huagongshe.com/reaction/1047749

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
ReactantMethanaminium, N-((dimethylamino)(3H-1,2,3-triazolo(4,5-b)pyridin-3-yloxy)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1)HCID 9886157—
Reactant2-Isopropoxy-3-methyl-benzoic acidHCID 59314088—
ReactantEthyl 2-amino-5-fluoro-2,3-dihydro-1H-indene-2-carboxylateHCID 59314154—
SolventDimethylformamideHCID 6228—
Product5-Fluoro-2-(2-isopropoxy-3-methyl-benzoylamino)-indan-2-carboxylic acid ethyl esterHCID 5931440286.2%

Reaction Steps

To a solution of 2-isopropoxy-3-methyl-benzoic acid (400 mg, 2.06 mmol), 2-amino-5-fluoro-indan-2-carboxylic acid ethyl ester (554 mg, 2.47 mmol), HATU 1.17 g, 3.09 mmol) in anhydrous DMF (10 mL) is added DIPEA (511 μL, 3.09 mmol). The resulting solution is stirred at RT overnight. After the removal of DMF in vacuo, the residue is dissolved in EtOAc (100 mL) and washed with water (1×10 mL) and brine (2×10 mL). The organic layer is dried over anhydrous Na2SO4 and concentrated in vacuo. The residue is purified by flash column chromatography (120 g silica gel, gradient elution: 5%-50% EtOAc in heptane) to give a pure product (96) as white solid (709 mg, 86%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08569535B2
Source datasetuspto-grants-2013_10
ORD IDord-af522f4e73754405aa2b52a047e1edb0
Source noteuspto-grants-2013_10