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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1047810Generated: November 1, 2026

Diisopropylethylamine → 2-[(5-Chloro-benzo[b]thiophene-3-carbonyl)-amino]-indane-2-carboxylic acid ethyl ester

https://huagongshe.com/reaction/1047810

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
ReactantMethanaminium, N-((1H-benzotriazol-1-yloxy)(dimethylamino)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1)HCID 2733084—
Reactant5-Chloro-benzo[b]thiophene-3-carboxylic acidHCID 2794574—
ReactantEthyl 2-amino-2,3-dihydro-1H-indene-2-carboxylateHCID 10921653—
SolventDichloromethaneHCID 6344—
SolventDichloromethane methanolHCID 21226129—
Product2-[(5-Chloro-benzo[b]thiophene-3-carbonyl)-amino]-indane-2-carboxylic acid ethyl esterHCID 5931418296.3%

Reaction Steps

To a 40 mL vial containing a stirring bar, 5-chloro-benzo[b]thiophene-3-carboxylic acid (518 g, 2.44 mmol) is charged with dry DCM (7 mL). Stirring is initiated. HBTU (922 mg, 2.43 mmol) and DIPEA (0.95 mL, 8.0 mmol) are added. Then 2-aminoindane-2-carboxylic acid ethyl ester (500 mg, 2.44 mmol) is added. The reaction is allowed to stir for 20 h. Analysis by tlc of the reaction mixture (silica, 10% MeOH/DCM) indicates complete consumption of the starting amine. The contents of the reaction flask are diluted with EtOAc (50 mL) and transferred to a separatory funnel. This is washed consecutively with dilute aqueous NaHCO3 (25 mL) and brine (25 mL), dried over MgSO4, filtered and evaporated in vacuo to provide 1.64 g of off white solid. This material is purified utilizing an ISCO Companion with a 40 g cartridge of silica. The gradient is 20% EtOAc in heptanes over 3 column volumes followed by a linear gradient to 50% over 8 column volumes and then 90% EtOAc for 2 column volumes with a ramp of 1 column volume. 25 mL fractions are collected. Fractions 7 through 31 are combined and evaporated in vacuo. Pumping to a constant weight gives amorphous white solid 0.94 g.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08569535B2
Source datasetuspto-grants-2013_10
ORD IDord-b2b9bcd6184441eb826717ae6c4d056f
Source noteuspto-grants-2013_10