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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 453704Generated: October 30, 2026

Ethyl chloroformate → HCID 86660314, compound

https://huagongshe.com/reaction/453704

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl chloroformateHCID 10928—
ReactantHCID 86660313HCID 86660313—
SolventDichloromethaneHCID 6344—
ProductHCID 86660314HCID 8666031420.6%

Reaction Steps

Ethyl carbonochloridate (10.5 μl, 0.11 mmol) was added to a solution of (R)-1-(2-(4-aminophenyl)-2-oxoethyl)-3-((R)-2-phenyl-2-(phenylamino)acetoxy)-1-azoniabicyclo[2.2.2]octane bromide (diastereomer 1 of I74) (60 mg, 0.11 mmol) in TEA (15.2 μl, 0.11 mmol) and DCM (2 mL). The reaction mixture was stirred at room temperature overnight. The solvent was evaporated under reduced pressure, and the product was purified by preparative HPLC (eluents: CH3CN/H2O) to obtain (R)-1-(2-(4-(ethoxycarbonylamino)phenyl)-2-oxoethyl)-3-((R)-2-phenyl-2-(phenylamino)acetoxy)-1-azoniabicyclo[2.2.2]octane bromide (14 mg, 20.6% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08492548B2
Source datasetuspto-grants-2013_07
ORD IDord-b585d1433bfd4f6d9866fd76aff22add
Source noteuspto-grants-2013_07