HuagongsheHuagongshe Chemistry Print Report · For research reference only
HCID 69654876, compound → HCID 69654705, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | HCID 69654876 | HCID 69654876 | — |
| Reactant | N-[4-(4-Oxo-1-piperidinyl)phenyl]-1-butanesulfonamide | HCID 86584570 | — |
| Product | HCID 69654705 | HCID 69654705 | — |
Reaction Steps
The title compound was prepared from butane-1-sulfonic acid [4-(4-oxo-piperidine-1-yl)-phenyl]-amide (which was obtained in Example 228) and N-[5-((2S)-3-amino-2-hydroxy-propoxy)-2-hydroxy-phenyl]-benzenesulfonamide (which was obtained in Example 21) according to the procedure of Example 278 as an off-white solid; 1H NMR (300 MHz, DMSO-d6) δ 0.83 (t, J=7.3 Hz, 3H), 1.20-1.40 (m, 4H), 1.55-1.70 (m, 2H), 1.80-1.95 (m, 2H), 2.50-2.80 (m, 5H), 2.92 (t, J=7.6 Hz, 2H), 3.50-3.90 (m, 5H), 6.39 (d, J=8.7, 2.9 Hz, 1H), 6.57 (d, J=8.7 Hz, 1H), 6.72 (d, J=2.9 Hz, 1H), 6.90 (d, J=9.0 Hz, 2H), 7.05 (d, J=9.0 Hz, 2H), 7.40-7.60 (m, 3H), 7.74 (d, J=7.7 Hz, 2H); MS (ES) m/z: 633.1 (MH+); HRMS Calcd. for C30H41N4O7S2 (MH+): 633.2411. Found: 633.2409.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06525202B2 |
| Source dataset | uspto-grants-2003_02 |
| ORD ID | ord-7bdeb049aa1648389f5d8fc5f3bb913a |
| Source note | uspto-grants-2003_02 |