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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 731520Generated: October 25, 2026

Hydrochloric Acid → HCID 131727621, compound

https://huagongshe.com/reaction/731520

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
Reactant4-MethylmorpholineHCID 7972—
ReactantDiisopropylcarbodiimideHCID 12734—
Reactant1-HydroxybenzotriazoleHCID 75771—
ReactantN2-((tert-Butoxy)carbonyl)-L-asparagineHCID 82035—
ReactantTert-butyl (2S)-2-amino-3-[4-(tert-butoxy)phenyl]propanoateHCID 7350495—
SolventDimethylformamideHCID 6228—
SolventDichloromethaneHCID 6344—
ProductHCID 131727621HCID 131727621—

Reaction Steps

Boc-Asn-OH (3.5 g 15 mmol) is dissolved in dichloromethane (100 ml amylene stabilised free of alcohol) and HOBt (2.24 g dry 16.5 mmol) is added. The mixture is cooled in an ice/water bath and DIC (2.45 ml 16 mmol) is added. The mixture will be allowed to react for 20 min. The HOBt on the bottom will react and a precipitate of DIU (on top) will form. H-Tyr(tBu)-OtBu×HCl (5.1 g 15.4 mmol) is dissolved in DMF (30 ml dry). The dichloromethane mixture containing the activated ester is filtered from the DIU directly into the DMF solution. The combined mixture is cooled in ice/water and NMM (1.75 ml 15.8 mmol) is added. The mixture is allowed to react over night. The solvents will be removed in vacuo. Ethyl acetate 200 ml is added and a precipitate is removed and the solution is washed with citric acid (2×50 ml 10%), sodium hydrogen carbonate (2×50 ml saturated) and brine (2×50 ml). The solution is dried with magnesium sulfate and the solvent removed in vacuo ending at 0.2 mBar for 30 min. The raw product will be suspended in pentane (40 ml) and filtered from a precipitate of DIU. The pentane will be removed in vacuo yielding the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07585839B2
Source datasetuspto-grants-2009_09
ORD IDord-149181ff9f0b411ab915340f7bedcfde
Source noteuspto-grants-2009_09