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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1047809Generated: October 30, 2026

Diisopropylethylamine → 2-(2-Iodo-3-methyl-benzoylamino)-indan-2-carboxylic acid ethyl ester

https://huagongshe.com/reaction/1047809

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
ReactantMethanaminium, N-((1H-benzotriazol-1-yloxy)(dimethylamino)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1)HCID 2733084—
Reactant2-Iodo-3-methylbenzoic acidHCID 2759365—
ReactantEthyl 2-amino-2,3-dihydro-1H-indene-2-carboxylateHCID 10921653—
SolventDichloromethaneHCID 6344—
SolventIsopropanol methylene chlorideHCID 21966342—
Product2-(2-Iodo-3-methyl-benzoylamino)-indan-2-carboxylic acid ethyl esterHCID 5931415362.1%

Reaction Steps

A 100 mL round bottom flask is charged with 2-iodo-3-methylbenzoic acid (1.92 g, 7.31 mmol) and dry DCM (25 mL). A stirring bar is added and stirring is initiated. After 5 min, the HBTU (2.37 g, 7.31 mmol) is added. After 5 min, the 2-amino-indane-2-carboxylic acid ethyl ester (1.5 g, 7.31 mmol) is added followed by N,N-diisopropylethyl-amine (3.2 mL, 18.37 mmol). The reaction is allowed to stir for 118 h. Analysis by tlc of the reaction mixture (silica, 15% iPrOH/DCM) indicates complete consumption of the starting amine. The contents of the reaction flask are transferred to a separatory funnel and diluted with EtOAc (70 mL). This is washed dilute aqueous HCl (3%, 2×30 mL), saturated aqueous NaHCO3 (2×30 mL) and brine (30 mL), dried over MgSO4, filtered and evaporated in vacuo to provide 2.04 g of a white solid. This material is dissolved in 15 mL of DCM. This material is purified utilizing an ISCO Companion with a 40 g cartridge of silica. The gradient is 10% EtOAc in heptanes over 4 column volumes followed by a linear gradient to 50% EtOAc over 10 column volumes. 27 mL fractions of UV active eluent are collected. Fractions 10 through 15 are combined and evaporated in vacuo. Pumping to constant weight gives 1.04 g a white solid material.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08569535B2
Source datasetuspto-grants-2013_10
ORD IDord-e32bebfa0fcf4686910bb7c3e06f3e39
Source noteuspto-grants-2013_10