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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 727903Generated: October 31, 2026

Triethylamine → Rabeprazole

https://huagongshe.com/reaction/727903

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantSodium HydroxideHCID 14798—
Reactantm-Chloroperbenzoic acidHCID 70297—
ReactantRabeprazole-thioetherHCID 9949996—
SolventDiethyl EtherHCID 3283—
SolventDichloromethaneHCID 6344—
ProductRabeprazoleHCID 502979.7%

Reaction Conditions

Temperature-10 °C

Reaction Steps

5 g of 2-[{4-(3-methoxypropoxy)-3-methylpyridine-2-yl}methylthio]-1H benzimidazole was dissolved in a mixture comprising 100 ml of dichloromethane and 25 ml of diethyl ether to obtain a solution. 2.83 g of 85% m-chloroperbenzoic acid was added to this solution in portions at -45° C. After the completion of the reaction, 2 g of triethylamine was added to the reaction mixture and the obtained mixture was heated to -10° C., followed by the addition of 50 ml of 1N sodium hydroxide. The obtained mixture was stirred at a room temperature for 30 minutes. The obtained aqueous layer was washed with 20 ml of dichloromethane twice and adjusted to pH 11 with a 2M aqueous solution of ammonium acetate. The aqueous layer was extracted with 50 ml of dichloromethane thrice. The obtained dichloromethane layer was washed with 50 ml of a saturated aqueous solution of sodium hydrogencarbonate twide, dried over magnesium sulfate and distilled to remove the dichloromethane. The obtained oily product was crystallized from dichloromethane/ether to obtain 4.17 g of the title compound as a white crystal.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05045552
Source datasetuspto-grants-1991_09
ORD IDord-3a47d11242994397abf18716f3080c92
Source noteuspto-grants-1991_09