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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 251382Generated: October 25, 2026

1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimide → Ethyl 3-{[2-(4-morpholinyl)ethyl]oxy}benzoate

https://huagongshe.com/reaction/251382

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimideHCID 15908—
Reactanttert-Butyl carbazateHCID 70091—
Reactant1-HydroxybenzotriazoleHCID 75771—
Reactant3-(5-amino-4-benzoyl-1H-pyrazol-1-yl)-4-methylbenzoic acidHCID 11209438—
ReactantSodium chloride; waterHCID 57417360—
SolventDimethylformamideHCID 6228—
ProductEthyl 3-{[2-(4-morpholinyl)ethyl]oxy}benzoateHCID 5808903926%

Reaction Conditions

Temperature0 °C

Reaction Steps

To DMF (10 mL) at rt was added 3-(5-amino-4-benzoyl-pyrazol-1-yl)-4-methyl-benzoic acid 1 (0.50 g, 1.56 mmol, 1.0 eq), t-butylcarbazate (0.206 g, 1.56 mmol, 1.0 eq), EDCI (0.313 g, 1.63 mmol, 1.05 eq) and HOBt (0.238 g, 1.56 mmol, 1.0 eq). The reaction was stirred for 19 h, poured into brine (100 mL) and extracted with EtOAc (2×20 mL). The organic extracts were combined were washed with brine (1×20 mL). The brine layer was separated and extacted with EtOAc (1×10 mL). All organic extracts were combined dried over Na2SO4, filtered and concentrated in vacuo. This material was dissolved in CH2Cl2 (10 mL) and cooled to 0° C. TFA (3 mL) was added and the reaction mixture allowed to warm to rt over 2 h. The solvent was removed in vacuo to give crude solid which was triturated with EtOAc/ether (1/1) giving 2 (180 mg, 26%)as a light tan in color solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07863314B2
Source datasetuspto-grants-2011_01
ORD IDord-01c92dc9ae754fbfa8ce639352e63b35
Source noteuspto-grants-2011_01