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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1783447Generated: October 30, 2026

tert-Butyl methyl ether → Pyrazine-2-carboxamidine hydrochloride

https://huagongshe.com/reaction/1783447

Reaction equation

Participants

RoleNameHCIDCharge
Reactanttert-Butyl methyl etherHCID 15413—
ReactantAmmonium ChlorideHCID 25517—
ReactantPyrazinecarbonitrileHCID 73172—
ReactantSodium MethoxideHCID 10942334—
SolventMethanolHCID 887—
ProductPyrazine-2-carboxamidine hydrochlorideHCID 47089595%

Reaction Conditions

Temperature30 °C

Reaction Steps

To a solution of sodium methoxide (NaOCH3) (51.4 g, 0.952 mol) in methanol (3800 ml) there is added cyanopyrazine (1.00 KG, 9.53 mol) slowly at room temperature. The mixture is heated to 30° C. and stirred for 6 h. The mixture is cooled to 25° C. followed by the addition of ammonium chloride (NH4Cl) (572 g, 10.5 mol). The reaction mixture is stirred for 22 h and methyl t-butyl ether (4000 mL) is added and the mixture is stirred for 15 min forming a solid. The solid is filtered and washed with methyl t-butyl ether (2×1000 mL) then dried at 40° C./0-10 mmHg for 17 h to give white solid product (1435 g) in 95% yield with 95% HPLC purity. 1H NMR (DMSO-D6): δ 9.7 (bs, 3H), 9.49 (d, 1H, J=1.5 Hz), 9.04 (m, 1H), 8.93 (t, 1H, J=1.5 Hz)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07501423B2
Source datasetuspto-grants-2009_03
ORD IDord-a8b98767deda4894a482860eed95169e
Source noteuspto-grants-2009_03