HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2170003Generated: November 1, 2026
Methanol → 2-[(6-Methoxypyrazin-2-ylamino)methyl]phenol
https://huagongshe.com/reaction/2170003
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methanol | HCID 887 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | HCID 53250722 | HCID 53250722 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 2-[(6-Methoxypyrazin-2-ylamino)methyl]phenol | HCID 53250728 | — |
Reaction Steps
Introduced into a microwave tube are 363 mg (1.29 mmol) of 2-[(6-bromopyrazin-2-ylamino)methyl]phenol, prepared as described previously in Example 12, to which 3 ml of methanol and 103 mg (2.58 mmol, 2 eq) of sodium hydroxide are added. The reaction mixture is then heated for 30 mins in a microwave oven at 150° C. and is then diluted with 50 ml of ethyl acetate. The mixture is neutralized with an ammonium chloride solution to pH=7, decanted and the organic phase is washed twice with 50 ml of water. The organic phase is dried over magnesium sulphate, filtered, and concentrated to dryness. The residue is purified by chromatography over silica with, as eluent, heptane/ethyl acetate (7/3). 2-[(6-Methoxypyrazin-2-ylamino)methyl]phenol is obtained in the form of a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09050266B2 |
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| Source dataset | uspto-grants-2015_06 |
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| ORD ID | ord-23203c035d7f4028b25166ce670367ae |
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| Source note | uspto-grants-2015_06 |
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