HuagongsheHuagongshe Chemistry Print Report · For research reference only
(+)-Norepinephrine → HCID 69654609, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | (+)-Norepinephrine | HCID 5814 | — |
| Reactant | 4-Methoxy-N-[4-(4-oxo-piperidin-1-yl)-phenyl]benzenesulfonamide | HCID 22220556 | — |
| Product | HCID 69654609 | HCID 69654609 | — |
Reaction Steps
The title compound was prepared from 4-methoxy-N-[4-(4-oxo-piperidine-1-yl)-phenyl]-benzenesulfonamide (which was obtained in Example 218) and L-norepinephrine according to the procedure of Example 255 as a white solid; 1 H NMR (300 MHz, DMSO-d6) δ 1.40-1.55 (m, 2H), 1.90-2.05 (m, 2H), 2.50-3.00 (m, 5H), 3.50-3.75 (m, 2H), 3.79 (s, 3H), 4.50-4.65 (m, 1H), 6.60 (d, J=8.0 Hz, 1H), 6.68 (d, J=8.0 Hz, 1H), 6.76-6.80 (m, 3H), 6.88 (d, J=9.0 Hz, 2H), 7.04 (d, J=7.8 Hz, 2H), 7.61 (d, J=7.8 Hz, 2H), 8.85 (s, 1H); MS (ES) m/z: 513.9 (MH+); HRMS Calcd. for C26H32N3O6S(MH+): 514.2011. Found: 514.2000.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06525202B2 |
| Source dataset | uspto-grants-2003_02 |
| ORD ID | ord-f8bea31ea6d5419189f47dceac7963ad |
| Source note | uspto-grants-2003_02 |