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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2083807Generated: October 31, 2026

1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimide → HCID 131711081, compound

https://huagongshe.com/reaction/2083807

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimideHCID 15908—
Reactant1-HydroxybenzotriazoleHCID 75771—
ReactantL-Threonine, N-[(1,1-dimethylethoxy)carbonyl]-O-(phenylmethyl)-HCID 1549483—
Reactant(S)-Pyrrolidine-2-carboxamide monohydrochlorideHCID 12707183—
SolventTetrahydrofuranHCID 8028—
ProductHCID 131711081HCID 13171108161.4%

Reaction Conditions

Temperature-5 °C

Reaction Steps

BOC-Thr(Bzl)-OH (67.7 g.), H-Pro-NH2.HCl (33.0 g.) and HOBT (29.6 g.) were added in THF (220 ml.). WSC (40.0 ml.) was added thereto under cooling at -5° C., stirred for 1 hour at -5° C. and then overnight at room temperature. The reaction mixture was concentrated in vacuo and ethyl acetate (800 ml.) was added to the residue, which is then washed twice with 1 N HCl (400 ml.) and twice with 5% sodium bicarbonate solution (300 ml.) and water. After dehydration by anhydrous magnesium sulfate, the organic layer was concentrated in vacuo. The oily material was charged for silicagel (450 g.) column chromatography. Developing by a mixture of benzene - ethyl acetate (1:1), ethyl acetate and methanol is this order and eluting fractions were checked by silica gel thin layer chromatography. Active fractions were collected and dissolved in ethyl acetate (500 ml.) then washed twice with 5% aqueous sodium bicarbonate (300 ml.) and water, and after drying with anhydrous magnesium sulfate, concentrated in vacuo. The residue was treated with n-hexane to obtain BOC-Thr-(Bzl)-Pro-NH2 as white powder (54.5 g., Yield: 61.4%). Rf1 = 0.48, [α]D28 = -14.0° (c=1, DMF).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04086221
Source datasetuspto-grants-1978_04
ORD IDord-b540d07223304f2aa016e3eac104798e
Source noteuspto-grants-1978_04