Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1047815Generated: November 2, 2026

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

https://huagongshe.com/reaction/1047815

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
ReactantBenzo(b)thiophene-3-carboxylic acidHCID 601280—
ReactantMethanaminium, N-((1H-benzotriazol-1-yloxy)(dimethylamino)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1)HCID 2733084—
ReactantEthyl 2-amino-2,3-dihydro-1H-indene-2-carboxylateHCID 10921653—
SolventDichloromethaneHCID 6344—
SolventDichloromethane methanolHCID 21226129—
Product2-[(Benzo[b]thiophene-3-carbonyl)-amino]-indane-2-carboxylic acid ethyl esterHCID 5931436577.4%

Reaction Steps

To a 40 mL vial containing a stirring bar, benzo[b]thiophene-3-carboxylic acid ([5381-25-9], 434 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. The 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 reparatory 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 4 through 16 are combined and evaporated in vacuo. Pumping to a constant weight gives amorphous white solid 0.69 g.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08569535B2
Source datasetuspto-grants-2013_10
ORD IDord-537364c9b3824b0197849e7387c64425
Source noteuspto-grants-2013_10