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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2273088Generated: November 2, 2026

Triethylamine → N-(6-Methoxy-2-pyrazinyl)-Na(2)-[4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]urea

https://huagongshe.com/reaction/2273088

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantTriphosgeneHCID 94429—
Reactant4-(Tetramethyl-1,3,2-dioxaborolan-2-yl)anilineHCID 2734620—
Reactant6-Methoxypyrazin-2-amineHCID 4868193—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
ProductN-(6-Methoxy-2-pyrazinyl)-Na(2)-[4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]ureaHCID 8971452528.2%

Reaction Steps

A mixture of 350 mg (1.60 mmol) of 4-(4,4,5,5-tetramethyl-[1,3,2]dioxaborolan-2-yl)phenylamine and 1.35 ml (9.59 mmol) of triethylamine in 10 ml of DCM is added, under nitrogen, to a solution of 474.07 mg (1.60 mmol) of triphosgene in 30 ml of DCM. The mixture is stirred for 30 minutes at room temperature, followed by addition of 1 g (7.99 mmol) of 6-methoxypyrazin-2-amine. The resulting mixture is stirred for 2 hours at room temperature. Water is added and the product is extracted with DCM. The solution is dried over MgSO4 and then filtered. The filtrate is evaporated under reduced pressure and the residue is then chromatographed on silica gel, eluting with a DCM/MeOH mixture from (100/0 v/v) up to (96/4 v/v). The solvent is evaporated off under reduced pressure. The residue is taken up in ethyl acetate and washed three times with 1N hydrochloric acid solution and then with saturated NaCl solution. The resulting solution is dried over MgSO4. 167 mg of 1-(6-methoxypyrazin-2-yl)-3-[4-(4,4,5,5-tetramethyl-[1,3,2]dioxaborolan-2-yl)phenyl]urea are obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09120812B2
Source datasetuspto-grants-2015_09
ORD IDord-1b53a6a027bc4a43b9f6cad3a5c3a095
Source noteuspto-grants-2015_09