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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 875450Generated: October 30, 2026

1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimide → HCID 71061557, compound

https://huagongshe.com/reaction/875450

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimideHCID 15908—
Reactant3-Amino-1,2-propanediolHCID 73561—
Reactant1-HydroxybenzotriazoleHCID 75771—
ReactantSodium BicarbonateHCID 516892—
ReactantHCID 71061723HCID 71061723—
SolventDimethylformamideHCID 6228—
ProductHCID 71061557HCID 7106155755.5%

Reaction Steps

To a solution of 3,5-dichloro-4-({7-[(cyclopropylcarbonyl)amino]-1H-pyrrolo[2,3-c]pyridin-3-yl}carbonyl)benzoic acid (50 mg, 0.11 mmol) in dimethylformamide (3 mL), 1-ethyl-3-(3-dimethylaminopropyl) carbodiimide (27.4 mg, 0.14 mmol), 1-hydroxybenzotriazole (19.37 mg, 0.14 mmol) and 3-aminopropane-1,2-diol (13 mg, 0.14 mmol) were added in one lot at room temperature. The resulting reaction mixture was stirred at room temperature for about 5 hours. Saturated aquoues sodium bicarbonate solution (20 mL) was added to quench the reaction mass. The aquoues phase was extracted with ethyl acetate and the combined organic layer dried over anhydrous sodium sulfate, filtered and concentrated. The crude product was purified by silica gel (100-200) column chromatography using ethyl acetate and hexane gradient elution to afford 3,5-dichloro-4-({7-[(cyclopropylcarbonyl)amino]-1H-pyrrolo[2,3-c]pyridin-3-yl}carbonyl)-N-(2,3-di hydroxypropyl)benzamide (30 mg, 51.72%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08980911B2
Source datasetuspto-grants-2015_03
ORD IDord-fd92d8fd7f6e4839abc9a8cf3b55f00f
Source noteuspto-grants-2015_03