HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-Aminophenol → HCID 135964711, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-Aminophenol | HCID 403 | — |
| Reactant | Trifluoroacetic acid | HCID 6422 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | HCID 11184602 | HCID 11184602 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Solvent | (+-)-2-Butanol | HCID 6568 | — |
| Product | HCID 135964711 | HCID 135964711 | — |
Reaction Steps
A mixture of 4-aminophenol (42 mg, 0.38 mmol), 1-chloro-4-(4-methylpiperazin-1-yl)phthalazine (100 mg, 0.381 mmol), and TFA (29 μl, 0.38 mmol) was heated in 2-butanol (3 mL) in a sealed tube at 90° C. overnight. Next day LC/MS shows completion of reaction. The reaction was cooled and diluted with DCM. Aqueous sodium bicarbonate was added and the organic layer was collected. The aqueous layer was neutralized with 1N HCl and the product was extracted with DCM. The organic layers were combined, dried over sodium sulfate, and concentrated to afford 4-(4-(4-methylpiperazin-1-yl)phthalazin-1-ylamino)phenol as solid brown material. MS [M+H]=336.2. Calc'd for C19H21N5O: 335.4.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07981891B2 |
| Source dataset | uspto-grants-2011_07 |
| ORD ID | ord-5f497908eb58472bb6ee22a77a2c308d |
| Source note | uspto-grants-2011_07 |