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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2205708Generated: October 29, 2026

Hydrochloric Acid → HCID 86720831, compound

https://huagongshe.com/reaction/2205708

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantDiethyl EtherHCID 3283—
ReactantHCID 86720832HCID 86720832—
ReactantHCID 86720833HCID 86720833—
Solvent1,4-DioxaneHCID 31275—
ProductHCID 86720831HCID 8672083199%

Reaction Steps

The 5-((3-((S)-phenyl(((R)-quinuclidin-3-yloxy)carbonylamino)methyl)phenoxy)-methyl)furan-2-carboxylic acid prepared as described in Example 6 Step 1 was further purified by reverse phase column chromatography eluting with gradient of Eluent A: Water/ACN 95/5+0.1% HCOOH and Eluent B: ACN/water 95/5+0.1% HCOOH. 5-((3-((S)-phenyl(((R)-quinuclidin-3-yloxy)carbonylamino)methyl)phenoxy)methyl)furan-2-carboxylic acid formate (1:1) (8.36 g, 16.12 mmol) was dispersed in Dioxane (50 mL) and then 4M HCl in dioxane (16.12 mL, 64.5 mmol) was added at 0° C. and the mixture stirred at it for 10 minutes until complete dissolution. The above mentioned solution was dropped in a 500 mL of Et2O under vigorous stirring to give a white precipitate that was collected by filtration. After drying under vacuum 5-((3-((S)-phenyl(((R)-quinuclidin-3-yloxy)carbonylamino)methyl)phenoxy)methyl)furan-2-carboxylic acid hydrochloride (8.2 g, 15.98 mmol, 99% yield) was isolate as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09371318B2
Source datasetuspto-grants-2016_06
ORD IDord-35b186e1d26e488f8e38d559335a1306
Source noteuspto-grants-2016_06