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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | tert-Butyl methyl ether | HCID 15413 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | Pyrazinecarbonitrile | HCID 73172 | — |
| Reactant | Sodium Methoxide | HCID 10942334 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | Pyrazine-2-carboxamidine hydrochloride | HCID 470895 | 95% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07501423B2 |
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| Source dataset | uspto-grants-2009_03 |
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| ORD ID | ord-a8b98767deda4894a482860eed95169e |
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| Source note | uspto-grants-2009_03 |
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