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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 220418Generated: October 26, 2026

Potassium Carbonate → 3'-m-Tolyl-2,3,5,6-tetrahydro-[1,2']bipyrazinyl-4-carboxylic acid t-butyl ester

https://huagongshe.com/reaction/220418

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant3-Tolylboronic acidHCID 2733950—
ReactantTert-butyl 4-(3-chloropyrazin-2-yl)piperazine-1-carboxylateHCID 11150691—
CatalystTetrakis(triphenylphosphine)palladiumHCID 11979704—
SolventWaterHCID 962—
Solvent1,2-DimethoxyethaneHCID 8071—
Product3'-m-Tolyl-2,3,5,6-tetrahydro-[1,2']bipyrazinyl-4-carboxylic acid t-butyl esterHCID 6873681247%

Reaction Steps

Dissolve 3′-chloro-2,3,5,6-tetrahydro-[1,2′]bipyrazinyl-4-carboxylic acid t-butyl ester (6.0 g, 20.2 mmol) and 3-methylbenzeneboronic acid (3.3 g, 24.0 mmol) in dimethoxyethane (20 mL) and water (10 mL). Add tetrakis(triphenylphosphine) palladium(0) (2.3 g, 2.0 mmol) and potassium carbonate (7.5 g, 54 mmol). Heat for 17 hr. at 102° C. and allow to cool about 1.5 hr. to room temperature. Partition reaction mixture between ethyl acetate and water. Separate layers. Wash organic layer with brine, dry (sodium sulfate), filter, concentrate and purify (silica gel chromatography eluting with 10:90 to 20:80 ethyl acetate:hexanes), to give 3′-m-tolyl-2,3,5,6-tetrahydro-[1,2′]bipyrazinyl-4-carboxylic acid t-butyl ester (3.3 g, 47%). MS (ES): m/z=355 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08202873B2
Source datasetuspto-grants-2012_06
ORD IDord-67c6e63518c046a48b58480b6132fa8a
Source noteuspto-grants-2012_06