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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2248440Generated: October 25, 2026

Triethylamine → N-methoxycarbonyl-5,6-methylenedioxy-2-[[(4-methoxy-3,5-dimethyl-2-pyridinyl)methyl]sulfinyl]-1H-benzimidazole

https://huagongshe.com/reaction/2248440

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantChloro methylformateHCID 12616564—
Reactant5,6-methylenedioxy-2-[[(4-methoxy-3,5-dimethyl-2-pyridinyl)methyl]sulfinyl]-1H-benzimidazoleHCID 21295863—
SolventDichloromethaneHCID 6344—
ProductN-methoxycarbonyl-5,6-methylenedioxy-2-[[(4-methoxy-3,5-dimethyl-2-pyridinyl)methyl]sulfinyl]-1H-benzimidazoleHCID 199964946%

Reaction Steps

Chloro methylformate (0.24 g, 0.0026 mol) dissolved in CH2Cl2 (5 ml) was added dropwise to a stirred solution of 5,6-methylenedioxy-2-[[(4-methoxy-3,5-dimethyl-2-pyridinyl)methyl]sulfinyl]-1H-benzimidazole (0.80 g, 0.0022 mol) and triethylamine in CH2Cl2 (10 ml). The mixture was then stirred at room temperature for 19 h. The CH2Cl2 -solution was washed with water, dried (MgSO4) and the solvent was evaporated giving the desired product as an oil (0.06 g, 6%). NMR data for the final product is given below.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05039806
Source datasetuspto-grants-1991_08
ORD IDord-b0a0a202695f4d1ba74cd04fb694d5ff
Source noteuspto-grants-1991_08