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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 376549Generated: October 28, 2026

Hydrochloric Acid → HCID 178490233, compound

https://huagongshe.com/reaction/376549

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantSodium BicarbonateHCID 516892—
ReactantHCID 54085635HCID 54085635—
ReactantHCID 178512549HCID 178512549—
SolventMethanolHCID 887—
SolventWaterHCID 962—
Solvent1,4-DioxaneHCID 31275—
SolventHCID 178418361HCID 178418361—
ProductHCID 178490233HCID 178490233—

Reaction Steps

In 5 ml of methanol was dissolved 250 mg of (S,S)-3-(3-aminopropyl)-4-[2-benzyloxycarbonylamino-3-(4-methoxyphenyl)propionyl]-2-oxopiperazine-1-acetic acid produced in Reference Example 36. To the solution was added 100 mg of 10% Pd--C, and the mixture was stirred for one hour at room temperature in hydrogen atmosphere. The catalyst was filtered off, and the filtrate was concentrated under reduced pressure to leave an oily substance. The oily substance was dissolved in a mixture of 10 ml of dioxane and 10 ml of water. To the solution were added 210 mg of sodium hydrogencarbonate and 450 mg of 4-guanidinobenzoic acid 3,5-dioxo-4-azatricyclo[5,2,1,0 2,6]deca-8-en-4-ylester. The mixture was stirred for one hour at room temperature. The pH of the reaction mixture was adjusted to 3 with 1N HCl, then dioxane was distilled off under reduced pressure. The remaining aqueous solution was subjected to a CHP-20 column. The fraction eluted with 10% acetonitrile/water was freeze-dried to afford 130 mg of the title compound as an amorphous powdery product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06020334
Source datasetuspto-grants-2000_02
ORD IDord-53e1c61ccf5c42a7aa8197a14a72c8f1
Source noteuspto-grants-2000_02