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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1982339Generated: October 30, 2026

Dicyclohexylcarbodiimide → HCID 178446040, compound

https://huagongshe.com/reaction/1982339

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDicyclohexylcarbodiimideHCID 10868—
Reactant1-HydroxybenzotriazoleHCID 75771—
ReactantZ-Sta-OHHCID 14560231—
ReactantHCID 178511197HCID 178511197—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
ProductHCID 178446040HCID 178446040—

Reaction Steps

370 mg of Z-Sta-OH, 225 mg of H-β-Ala-His-NH2, 153 mg of HOBt×H2O and 247 mg of DCCI are suspended in 4.5 ml of DMF and stirred at room temperature. After approximately 10 minutes a clear solution has formed and afrer approximately 20 minutes DCH begins to crystallize out. The mixture is left to stand overnight, then stirred for 30 minutes at 0°, DCH is filtered off und the filtrate is concentrated to an oil. This is heated for 1 hour at 60° in 14 ml of methanol/glacial acetic acid/H2O (94:3:3), the solution is concentrated to 3 ml and the crude product is precipitated by 30 ml of diisopropyl ether and dried. To remove the acetic acid, the residue is dissolved in n-butanol, washed in succession with 5% strength NaHCO3 solution and with water, and the butanol phase is again concentrated to dryness. After purification by chromatography over 30 g of silica gel (Merck No. 60, 230-400 mesh) using as eluant chloroform/methanol (75:25), Z-Sta-β-Ala-His-NH3 is obtained; Rf (G)=0.28.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04595677
Source datasetuspto-grants-1986_06
ORD IDord-20240a15e979448e823e073bc5cae017
Source noteuspto-grants-1986_06