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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 275889Generated: October 30, 2026

1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimide → HCID 54466640, compound

https://huagongshe.com/reaction/275889

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimideHCID 15908—
Reactant1-HydroxybenzotriazoleHCID 75771—
ReactantDiisopropylethylamineHCID 81531—
ReactantGlycine methyl ester hydrochlorideHCID 122755—
Reactant3-Methoxy-4-o-tolylureidophenylacetic acidHCID 11449840—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
SolventDichloromethaneHCID 6344—
ProductHCID 54466640HCID 5446664064.7%

Reaction Steps

A stirred solution of [3-methoxy-4-(3-o-tolylureido)phenyl]-acetic acid (7.53 g, Reference Example 5) in a mixture of dimethylformamide (15 ml) and dichloromethane (150 ml) was treated with 1-(3-dimethylaminoprop-1-yl)-3-ethylcarbodiimide (4.98 g), then with 1-hydroxybenzotriazole (3.57 g), then with glycine methyl ester hydrochloride (3.01 g) and then with diisopropylethylamine (4.10 ml). After stirring at room temperature for 20 hours the reaction mixture was diluted with water (100 ml). The organic phase was washed with saturated sodium bicarbonate (100 ml), then with hydrochloric acid (1M) and then with brine, then dried over magnesium sulphate and then evaporated. The residue was triturated with petroleum ether and the resulting cream coloured solid (6.25 g) was dissolved in tetrahydrofuran (200 ml). The solution was treated with water (50 ml) and then with lithium hydroxide hydrate (0.75 g). The mixture was stirred at room temperature for 4 hours and then the tetrahydrofuran was removed under vacuum. The aqueous phase was acidified by addition of hydrochloric acid (12M). The resulting solid was washed with diethyl ether and then dried to give the title compound (5.76 g), m. p. 130-134° C. (with decomposition). MS: 370 [M−1]−. HPLC: RT=10.16 minutes (gradient clution using a mixture of acetonitrile and water 4:1 to 1:4 v/v).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06352977B1
Source datasetuspto-grants-2002_03
ORD IDord-c3c490f3226e44e4aecb05dff9836ce9
Source noteuspto-grants-2002_03