HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2062148Generated: November 1, 2026
Piperazine → 2-(4-(Piperazin-1-yl)quinazolin-2-yl)phenol
https://huagongshe.com/reaction/2062148
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Piperazine | HCID 4837 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 2-(4-Chloroquinazolin-2-yl)phenol | HCID 4050956 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 2-(4-(Piperazin-1-yl)quinazolin-2-yl)phenol | HCID 136105362 | 83% |
Reaction Steps
To a solution of 2-(4-chloroquinazolin-2-yl)phenol (2.0 g, 7.8 mmol) in CH2Cl2 at 0° C. was rapidly added a solution of piperazine (2.01 g, 23.4 mmol) and triethylamine (2.17 mL, 15.6 mmol) in 10 mL CH2Cl2. The reaction was warmed to room temperature and stirred for 5 hours. The reaction was quenched with 25 mL of water and extracted with (3×15) mL of CH2Cl2. The organic layer was dried over Na2SO4, filtered, and concentrated to afford 2-(4-(piperazin-1-yl)quinazolin-2-yl)phenol (1.98 g, 83%). LC/MS: m/z 307.3 (M+H)+ at 1.47 min (10%-99% CH3CN (0.035% TFA)H2O (0.05% TFA)). 1H NMR (400 MHz, DMSO-d6) δ 8.43 (d, J=10.1 Hz, 1H), 8.04 (d, J=8.3 Hz, 1H), 7.85 (m, 2H), 7.53 (m, 1H), 7.38 (m, 1H), 6.95 (m, 2H), 3.85 (t, J=4.8 Hz, 4H), 2.94 (t, J=4.8 Hz, 4H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08283354B2 |
|---|
| Source dataset | uspto-grants-2012_10 |
|---|
| ORD ID | ord-d85021124c96424baa401bda5dcd340a |
|---|
| Source note | uspto-grants-2012_10 |
|---|