HuagongsheHuagongshe Chemistry Print Report · For research reference only
1-(3,4-Xylyl)piperazine → HCID 10067089, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1-(3,4-Xylyl)piperazine | HCID 2723782 | — |
| Reactant | 5-Isocyanatoisoquinoline | HCID 11586357 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | HCID 10067089 | HCID 10067089 | — |
Reaction Steps
1-(3,4-Dimethylphenyl)piperazine (194 mg, 1.02 mmol) in diethyl ether (20 mL) was treated with an ethereal solution of 5-isocyanatoisoquinoline. The precipitate that formed was collected by filtration, washed with diethyl ether, and air-dried to provide the title compound. 1H NMR (300 MHz, DMSO-d6) δ 9.29 (d, 1H, J=0.7 Hz), 8.82 (s, 1H), 8.49 (d, J=6.2 Hz, 1H), 7.90-7.93 (m, 1H), 7.76-7.79 (m, 1H), 7.61-7.71 (m, 2H), 7.00 (d, 1H, 8.5 Hz), 6.83 (d, 1H, J=2.4 Hz), 6.73 (dd, 1H, J=8.3 Hz, 2.5 Hz), 3.67 (m, 4H), 3.15 (m, 4H), 2.19 (s, 3H), 2.13 (s, 3H); MS (ESI+) m/z 361 (M+H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06933311B2 |
| Source dataset | uspto-grants-2005_08 |
| ORD ID | ord-ce01c0a99db74e658cc1af1eb7e2df17 |
| Source note | uspto-grants-2005_08 |