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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1197002Generated: October 30, 2026

1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimide → HCID 22844257, compound

https://huagongshe.com/reaction/1197002

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimideHCID 15908—
Reactant1-HydroxybenzotriazoleHCID 75771—
ReactantGlycine ethyl ester, hydrochlorideHCID 2723640—
ReactantN-(tert-Butoxycarbonyl)-3-[(triphenylmethyl)sulfanyl]-L-valineHCID 15000273—
SolventWaterHCID 962—
SolventChloroformHCID 6212—
SolventTetrahydrofuranHCID 8028—
SolventTriethylamineHCID 8471—
ProductHCID 22844257HCID 2284425799%

Reaction Steps

To the solution of N-t-butoxycarbonyl-S-trityl-L-penicillamine (A-1) (4.0 g) and 1-hydroxybenzotriazole (abbreviated as HOBt) (1.2 g) in chloroform (40 ml) and tetrahydrofuran (16 ml), was added dropwise by ice-cooling the solution of 1-ethyl-3-(3dimethylaminopropyl)carbodiimide (water-soluble carbodiimide: abbreviated as WSC) (1.7 g) in chloroform (10 ml). The mixture was stirred at the same temperature for 1 hour, then glycine ethyl ester hydrochloride (1.1 g) and triethylamine (0.85 ml) were added, and the mixture was stirred at room temperature for 12 hours. After addition of water, the organic layer was washed with an aqueous solution of potassium hydrogensulfate, water, an aqueous solution of sodium hydrogencarbonate, water and saturated saline, in this order, and dried over magnesium sulfate. The solvent was evaporated off under reduced pressure, and the residue was subjected to column chromatography, to give N-t-butoxycarbonyl-S-trityl-L-penicillamylglycine ethyl ester (4.5 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05116861
Source datasetuspto-grants-1992_05
ORD IDord-f6d32edeb5b5411fa6745c530055f91b
Source noteuspto-grants-1992_05