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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2170002Generated: October 29, 2026

Dimethyl Sulfoxide → HCID 53250722, compound

https://huagongshe.com/reaction/2170002

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethyl SulfoxideHCID 679—
Reactant2-(Aminomethyl)phenolHCID 70267—
Reactant1,8-Diazabicyclo(5.4.0)undec-7-eneHCID 81184—
Reactant2,6-DibromopyrazineHCID 20361700—
SolventEthyl AcetateHCID 8857—
ProductHCID 53250722HCID 53250722—

Reaction Steps

Introduced into a 50 ml round-bottomed flask is 1 g (4.2 mmol) of 2,6-dibromopyrazine (starting material 3), to which 15 ml of dimethyl sulphoxide, 638 mg (4.2 mmol, 1eq) of 1,8-diazabicyclo[5.4.0]undec-7-ene, and 1.03 g (8.4 mmol, 2 eq) of 2-hydroxybenzylamine (starting material 4) are added; the mixture is left stirring for 2 h at room temperature. The reaction medium is diluted with 50 ml of ethyl acetate and then the mixture is washed with 50 ml of a saturated solution of ammonium chloride, and then twice with 50 ml of water. The organic phases are dried over magnesium sulphate, filtered and concentrated to dryness. The residue is purified by chromatography over silica with, as eluent, a heptane/ethyl acetate (8/2) mixture. 2-[(6-Bromopyrazin-2-ylamino)methyl]phenol is obtained in the form of a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09050266B2
Source datasetuspto-grants-2015_06
ORD IDord-5135c05b7dde4f4bb1c52bbe13a6f158
Source noteuspto-grants-2015_06