HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2282095Generated: October 26, 2026
4-(5-Amino-6-(phenylmethyl)-2-pyrazinyl)phenol → 2-((3-Benzyl-5-(4-hydroxyphenyl)pyrazin-2-yl)amino)hexanoic acid
https://huagongshe.com/reaction/2282095
Participants
| Role | Name | HCID | Charge |
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| Reactant | 4-(5-Amino-6-(phenylmethyl)-2-pyrazinyl)phenol | HCID 193743 | — |
| Reactant | 2-ketohexanoic acid sodium salt | HCID 23669158 | — |
| Catalyst | Acetic Acid | HCID 176 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 2-((3-Benzyl-5-(4-hydroxyphenyl)pyrazin-2-yl)amino)hexanoic acid | HCID 136391034 | 46.1% |
Reaction Steps
4-(5-amino-6-benzylpyrazin-2-yl)phenol (200 mg, 0.72 mmol) was mixed with 2-Ketohexanoic acid sodium salt (220 mg, 1.44 mmol) in ethanol (20 mL). Pd/C (10% Palladium in active carbon, 100 mg) was added with a few drops of acetic acid, and the reaction mixture heated to 65° C. Air was bubbled out by N2 gas, and a hydrogen balloon applied to the reaction flask. The reaction was continuously stirred for 4 hrs. After cooling down, it was filtered and the resulting solution was purified by flash chromatography (eluting solvent: 50% EtOAc in heptanes) to give the product as a yellow powder (130 mg, 46%). MS (ESI): m/z 392.2 (M+1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09139836B2 |
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| Source dataset | uspto-grants-2015_09 |
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| ORD ID | ord-94d033af27114d499e86b1aa27dc9523 |
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| Source note | uspto-grants-2015_09 |
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