HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 906205Generated: October 30, 2026
Triethylamine → 2-Amino-3,6-dibromopyrazine
https://huagongshe.com/reaction/906205
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | P,P-Diphenylphosphinic azide | HCID 199401 | — |
| Reactant | 3,6-Dibromopyrazine-2-carboxylic acid | HCID 53302220 | — |
| Solvent | tert-Butanol | HCID 6386 | — |
| Product | 2-Amino-3,6-dibromopyrazine | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08012983B2 |
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| Source dataset | uspto-grants-2011_09 |
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| ORD ID | ord-f1ff70b0333c4601bfd6669ba7bb24cd |
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| Source note | uspto-grants-2011_09 |
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