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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1711573Generated: November 2, 2026

Lansoprazole → HCID 59769506, compound

https://huagongshe.com/reaction/1711573

Reaction equation

Participants

RoleNameHCIDCharge
ReactantLansoprazoleHCID 3883—
ReactantTriethylamineHCID 8471—
ReactantEthyl AcetateHCID 8857—
ReactantHCID 85900220HCID 85900220—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventTetrahydrofuranHCID 8028—
ProductHCID 59769506HCID 5976950667.8%

Reaction Conditions

Temperature60 °C

Reaction Steps

To a solution (10 mL) of 2-[(chlorocarbonyl)(phenyl)amino]ethyl acetate (0.58 g) prepared in the same manner as in Synthetic Example 25 in tetrahydrofuran were added 2-[[[3-methyl-4-(2,2,2-trifluoroethoxy)-2-pyridyl]methyl]sulfinyl]-1H-benzimidazole (0.739 g), triethylamine (0.558 mL) and 4-dimethylaminopyridine (0.024 g), and the mixture was stirred at 60° C. for 15 hrs. Ethyl acetate (30 mL) was added to the reaction mixture, and the mixture was washed with water (50 mL) and saturated brine (50 mL), dried over anhydrous sodium sulfate, and concentrated under reduced pressure. The residue was purified by flash silica gel column chromatography (eluted with acetone:hexane=1:4, then 3:2). Crystallization from diethyl ether gave the title compound (0.779 g) as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07790755B2
Source datasetuspto-grants-2010_09
ORD IDord-fc4048d45cd04d5b845934f5563b26af
Source noteuspto-grants-2010_09