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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 625647Generated: October 31, 2026

Hydrochloric Acid → HCID 178461866, compound

https://huagongshe.com/reaction/625647

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantHCID 178462196HCID 178462196—
SolventMethanolHCID 887—
Solvent1,4-DioxaneHCID 31275—
ProductHCID 178461866HCID 178461866—

Reaction Steps

A solution of 4N HCl in dioxane (10 mL) was added to tert-butyl ((1S)-1-(4-(4-(6-(2-((1S)-1-((tert-butoxycarbonyl)amino)ethyl)-1H-imidazol-4-yl)-2-naphthyl)phenyl)-1H-imidazol-2-yl)ethyl)carbamate (368 mg. 0.59 mmol) in MeOH (10 mL) and stirred at ambient conditions for 5 hours, concentrated, and dried under vacuum. Tetra HCl salt (assume theoretical: 334 mg). LC-MS retention time 1.33 min; calcd. for C26H27N6: 423.23 m/z Found 423.17 [M+H]+. LC data was recorded on a Shimadzu LC-10AS liquid chromatograph equipped with a PHENOMENEX® Luna 2.0×30 mm column using a SPD-10AV UV-Vis detector at a detector wave length of 220 nM. The elution conditions employed a flow rate of 1 mL/min, a gradient of 100% Solvent A/0% Solvent B to 0% Solvent A/100% Solvent B, a gradient time of 2 min, a hold time of 1 min and an analysis time of 3 min where Solvent A was 5% methanol/95% water/0.1% TFA and Solvent B was 95% methanol/5% water/0.1% TFA. MS data was determined using a MICROMASS® Platform for LC in electrospray mode.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09303007B2
Source datasetuspto-grants-2016_04
ORD IDord-d925e00a9633483eaaaf59a3c1047483
Source noteuspto-grants-2016_04