HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-Hydroxybenzylamine → 4-{[(3-Amino-6-bromopyrazin-2-yl)amino]methyl}phenol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-Hydroxybenzylamine | HCID 97472 | — |
| Reactant | 2-Amino-3,5-dibromopyrazine | HCID 620004 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Product | 4-{[(3-Amino-6-bromopyrazin-2-yl)amino]methyl}phenol | HCID 24820428 | 11.7% |
Reaction Steps
A solution of 3,5-dibromo-pyrazin-2-ylamine (220 mg, 0.87 mmol) and 4-aminomethyl-phenol (225.0 mg, 1.83 mmol) in DMSO (2.5 mL) was heated at 98° C. under nitrogen for 24 hours. HPLC showed that 35% of product was formed and 40% of starting material presented. The reaction solution was partitioned between EtOAc and water. After condensation of organic layer, the residue was purified on a silica gel column eluting with 3% methanol in dichloromethane to provide 4-[(3-amino-6-bromo-pyrazin-2-ylamino)-methyl]-phenol (30 mg) as a yellow solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07250417B2 |
| Source dataset | uspto-grants-2007_07 |
| ORD ID | ord-f54413153dba4639ab1ace9cd9bb69ca |
| Source note | uspto-grants-2007_07 |