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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1047763Generated: October 25, 2026

Diisopropylamine → 2-(3-Methyl-2-pent-1-ynyl-benzoylamino)-indan-2-carboxylic acid ethyl ester

https://huagongshe.com/reaction/1047763

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylamineHCID 7912—
Reactant1-PentyneHCID 12309—
Reactant2-(2-Iodo-3-methyl-benzoylamino)-indan-2-carboxylic acid ethyl esterHCID 59314153—
CatalystCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
CatalystHCID 178418397HCID 178418397—
SolventDimethylformamideHCID 6228—
Product2-(3-Methyl-2-pent-1-ynyl-benzoylamino)-indan-2-carboxylic acid ethyl esterHCID 5931418524%

Reaction Steps

To a solution of 2-(2-iodo-3-methyl-benzoylamino)-indan-2-carboxylic acid ethyl ester (693 mg, 1.54 mmol) in anhydrous DMF (5 mL) and DIPA (diisopropylamine, 10 mL) is added Pd(PPh3)4 (89 mg, 7.7% mmol), CuI (29 mg, 0.154 mmol) and pent-1-yne (1.5 mL, 15.4 mmol). The resulting solution is covered in argon and run in a microwave reaction: 110° C., 35 minutes. After the removal of DMF and DIPA 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: 0%-40% EtOAc in heptane) to give a pure product (122) as a pale yellow solid (144 mg, 24%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08569535B2
Source datasetuspto-grants-2013_10
ORD IDord-4ef08da1335d42d18ed9f84076b1da93
Source noteuspto-grants-2013_10