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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 83676Generated: October 30, 2026

1,2-Dichloroethane → 1-(1-(4-chlorobenzyl)-1H-indole-2-carbonyl)-N-((2,3-dihydro-1H-inden-1-yl)methyl)piperidine-4-carboxamide

https://huagongshe.com/reaction/83676

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,2-DichloroethaneHCID 11—
Reactant1-HydroxybenzotriazoleHCID 75771—
ReactantDiisopropylethylamineHCID 81531—
ReactantINDAN-2-YL-METHYLAMINE HYDROCHLORIDEHCID 54594123—
Reactant1-(1-(4-chlorobenzyl)-1H-indole-2-carbonyl)piperidine-4-carboxylic acidHCID 57385796—
SolventDichloromethaneHCID 6344—
SolventEthyl AcetateHCID 8857—
Product1-(1-(4-chlorobenzyl)-1H-indole-2-carbonyl)-N-((2,3-dihydro-1H-inden-1-yl)methyl)piperidine-4-carboxamideHCID 66571682—

Reaction Steps

The following was added sequentially to DCM (6 mL): 1-(1-(4-chlorobenzyl)-1H-indole-2-carbonyl)piperidine-4-carboxylic acid (134 mg, 0.340 mmol), DIPEA (0.178 mL, 1.019 mmol), EDC (78 mg, 0.408 mmol), HOBT (62.4 mg, 0.408 mmol), and 2-indanmethanamine hydrochloride (62 mg, 0.340 mmol). The mixture was stirred for 18 h at rt, at which time the solution diluted with a 1:1 solution of ethyl acetate:diethyl ether and washed with 1M HCl (1×), 10% aq. sodium carbonate (1×) and brine (1×). The organic phase was dried with magnesium sulfate and concentrated in vacuo. The resulting residue was dissolved in EtOAc and precipitated out hexanes, and then collected over a filter and washed with diethyl ether to give the title compound as a white solid. (Yield: 72 mg, 0.137 mmol, 41%) 1H NMR (400 MHz, CDCl3) 7.63, 7.32, 7.28-7.11, 7.01, 6.62, 5.45, 5.38, 4.36, 3.70-3.52, 3.51-3.07, 3.06-2.76, 2.30-2.19, 1.86-1.61, 1.49

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08846684B2
Source datasetuspto-grants-2014_09
ORD IDord-33db8dd020784bb8ad8beb42fdd38a83
Source noteuspto-grants-2014_09