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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 722987Generated: October 30, 2026

Hydrochloric Acid → HCID 178427559, compound

https://huagongshe.com/reaction/722987

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantDicyclohexylcarbodiimideHCID 10868—
Reactant1-HydroxybenzotriazoleHCID 75771—
ReactantN-(tert-butoxycarbonyl)glycineHCID 78288—
ReactantArg(Tos)-Pro-Ala-Lys(ClZ)-OBzlHCID 178427560—
SolventTetrahydrofuranHCID 8028—
SolventChloroform methanolHCID 21584188—
ProductHCID 178427559HCID 17842755973%

Reaction Conditions

Temperature0 °C

Reaction Steps

At 0° C. the solution of 930 mg (1.01 mmol) of HCl.Arg(Tos)-Pro-Ala-Lys(ClZ)-OBzl (SEQ ID NO: 12) in 15 ml of anhydrous tetrahydrofuran was adjusted to pH 9, to which the pre-cold solution of 200 mg (1.14 mmol) of Boc-Gly-OH, 150 mg (1.11 mmol) of 1-hydroxybenzotriazole and 235 mg (1.14 mmol) of dicyclohexylcarbodiimide in 40 ml of anhydrous tetrahydrofuran was added. The reaction mixture was stirred at 0° C. for 2 h and at room temperature for 12 h and TLC (chloroform/methanol, 10:1) indicated complete disappearance of HCl.Arg(Tos)-Pro-Ala-Lys(ClZ)-OBzl (SEQ ID NO: 12). The resulted precipitates of N,N-dicyclohexylurea were filtrated and the filtrate was diluted with 100 ml of ethyl acetate. The solution obtained was washed successively with saturated NaCO3 in water (50 ml×3), saturated NaCl in water (50 ml×3) and KHSO4 in water (5%, 50 ml×3). The separated ethyl acetate layer was dried with anhydrous MgSO4, and then evaporated. The residue was purified on sinica gel chromatography (CHCl3/CH3OH, 30/1) to provide 770 mg (73%) of the title compound as a glassy mass. Mp 82–84° C., FAB-MS (m/e) 1038.6[M+H]+, 1061.7[M+Na]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07138491B2
Source datasetuspto-grants-2006_11
ORD IDord-3e162a5a187041cfa4619ea109d1729b
Source noteuspto-grants-2006_11