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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 723008Generated: October 30, 2026

Hydrochloric Acid → HCID 178427590, compound

https://huagongshe.com/reaction/723008

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantDicyclohexylcarbodiimideHCID 10868—
Reactant1-HydroxybenzotriazoleHCID 75771—
ReactantL-Ornithine, N2-[(1,1-dimethylethoxy)carbonyl]-N5-[imino[[(4-methylphenyl)sulfonyl]amino]methyl]-HCID 83767—
ReactantArg(Tos)-Pro-Ala-Lys(ClZ)-OBzlHCID 178427560—
SolventTetrahydrofuranHCID 8028—
SolventChloroform methanolHCID 21584188—
ProductHCID 178427590HCID 17842759080%

Reaction Conditions

Temperature0 °C

Reaction Steps

At 0° C. the solution of 18 mg (0.075 mmol) of HCl Pro-OBzl in 5 ml of anhydrous tetrahydrofuran was adjusted to pH 9, to which the pre-cold solution of 33 mg (0.077 mmol) Boc-Arg(Tos)-OH, 10 mg (0.074 mmol) of 1-hydroxybenzotriazole and 16 mg (0.077 mmol) of dicyclohexylcarbodiimide in 10 ml of anhydrous tetrahydrofuran was added. The reaction mixture was stirred at 0° C. for 2 h and at room temperature for 5 h and TLC (chloroform/methanol, 30:1) 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 30 ml of ethyl acetate. The solution obtained was washed successively with saturated NaCO3 in water (10 ml×3), saturated NaCl in water (10 ml×3) and KHSO4 in water (5%, 10 ml×3). The separated ethyl acetate layer was dried with anhydrous MgSO4, filtered. The filtrate was evaporated to provide 37 mg (80%) of the title compound as a colorless powder. Mp 60–62° C., FAB-MS (m/e) 617[M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07138491B2
Source datasetuspto-grants-2006_11
ORD IDord-28c189e0bfbc43c988bbe1edd5b5c7c5
Source noteuspto-grants-2006_11