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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 906205Generated: October 30, 2026

Triethylamine → 2-Amino-3,6-dibromopyrazine

https://huagongshe.com/reaction/906205

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantP,P-Diphenylphosphinic azideHCID 199401—
Reactant3,6-Dibromopyrazine-2-carboxylic acidHCID 53302220—
Solventtert-ButanolHCID 6386—
Product2-Amino-3,6-dibromopyrazineHCID 51051665—

Reaction Steps

Diphenylphosphorylazide (2.59 mL, 12 mmol) and triethylamine (1.67 mL, 12 mmol) are added to a solution of 3,6-dibromo-pyrazin-2-carboxylic acid (3.52 g, 12 mmol) in t-butanol (90 mL). The reaction is heated at reflux for 18 hours. The reaction is quenched with water, then concentrated in vacuo and taken up in DCM. The organic solution is washed with water and 1N NaOH, dried over MgSO4 and concentrated in vacuo. The resultant solid is filtered through a pad of silica using EtOAc, then concentrated and TFA:DCM (4:1, 12 mL) is added to the solid and stirred for 30 min. The solution is concentrated in vacuo then neutralised with 1N NaOH and extracted with DCM. The organic layer is dried over anhydrous MgSO4 and concentrated in vacuo to give the product. 1H NMR (250 MHz, DMSO-d6) δ(ppm) 7.25 (br s, 2H), 7.68 (s, 1H); m/z (APCI) 254 (M+H)+; m.p 135-139° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08012983B2
Source datasetuspto-grants-2011_09
ORD IDord-f1ff70b0333c4601bfd6669ba7bb24cd
Source noteuspto-grants-2011_09