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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2082221Generated: October 28, 2026

Trifluoroacetic acid → HCID 131717765, compound

https://huagongshe.com/reaction/2082221

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantAnisoleHCID 7519—
Reactant1-HydroxybenzotriazoleHCID 75771—
Reactant1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
ReactantBoc-D-Trp(For)-OHHCID 7021874—
ReactantHCID 131717766HCID 131717766—
SolventDichloromethaneHCID 6344—
ProductHCID 131717765HCID 131717765—

Reaction Steps

To an ice-cooled solution of Boc-Phe-NEtBzl (3.95 g) and anisole (4 ml) in methylene chloride (16 ml) was added TFA (16 ml). The solution was stirred for an hour at room temperature. After evaporation, addition and re-evaporation of 4N-HCl/DOX (5 ml) were repeated twice. The residue was dissolved in DMF (40 ml), and the solution was ice-cooled and neutralized with triethylamine (1.39 ml). To the solution containing H-Phe-NEtBzl obtained was added Boc-D-Trp(CHO)-OH (3.32 g), HOBT (1.35 g) and WSC.HCl (1.92 g). The solution was stirred for one and half an hour at room temperature. After evaporation and extraction with ethyl acetate. The organic layer was washed successively with water, 2% hydrochloric acid, water, 2% sodium hydrogencarbonate, water and saturated sodium chloride and dried over magnesium sulfate. The evaporated residue was subjected to column chromatography on silica gel (200 g) and eluted with a mixture of chloroform and methanol (50:1 to 20:1, gradient elution). The fractions containing the object compound were combined and evaporated. The residue were pulverized with n-hexane, collected by filtration, washed with n-hexane and dried to give Boc-D-Trp(CHO)-Phe-NEtBzl (4.47 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05187156
Source datasetuspto-grants-1993_02
ORD IDord-1d097c52f8114f71b3b0bf284333c5e9
Source noteuspto-grants-1993_02