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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 420135Generated: October 29, 2026

1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimide → HCID 178492636, compound

https://huagongshe.com/reaction/420135

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimideHCID 15908—
Reactant1-HydroxybenzotriazoleHCID 75771—
Reactant1-cyclopropyl-4-methoxy-1H-indole-6-carboxylic acidHCID 66649403—
ReactantHCID 178513836HCID 178513836—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
ProductHCID 178492636HCID 178492636—

Reaction Steps

To a solution of 1-cyclopropyl-4-methoxy-1H-indole-6-carboxylic acid (54 mg) and 5-[4-oxo-spiro(chroman-2,4′-piperidin)-6-yl]-4H-1,2,4-triazole-3-carboxamide (102 mg) in DMF (4 mL) were added TEA (77 uL), HOBT (42 mg), and WSC (53 mg) at room temperature and the reaction mixture was stirred at room temperature overnight. The reaction mixture was poured into H2O, extracted with CHCl3, dried over sodium sulfate, filtered, and concentrated in reduced pressure. The residue was purified by column chromatography on silica gel using a mixture of CHCl3/MeOH (1:0-10:1) as eluent to give the title compound as a colorless solid. 1H-NMR (400 MHz, CDCl3) δ: 8.78-8.60 (1H, m), 8.40-8.25 (1H, m), 7.29 (1H, s), 7.15 (1H, d, J=8.0 Hz), 7.09 (1H, d, J=4.0 Hz), 6.57 (1H, s), 6.52 (1H, d, J=4.0 Hz), 4.30-4.17 (1H, m), 3.95 (3H, s), 3.62-3.38 (3H, m), 3.38-3.32 (1H, m), 2.85 (2H, s), 2.28-1.70 (4H, m), 1.06-1.04 (2H, m), 1.00-0.97 (2H, m); MS [M+H]+=541.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08093389B2
Source datasetuspto-grants-2012_01
ORD IDord-b4339f12e0aa4de497549e82acd6dc88
Source noteuspto-grants-2012_01