HuagongsheHuagongshe Chemistry Print Report · For research reference only
5-[4-(4-Oxo-piperidin-1-yl)-benzyl]-thiazolidine-2,4-dione → HCID 86584557, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 5-[4-(4-Oxo-piperidin-1-yl)-benzyl]-thiazolidine-2,4-dione | HCID 12965955 | — |
| Reactant | HCID 69654860 | HCID 69654860 | — |
| Product | HCID 86584557 | HCID 86584557 | — |
Reaction Steps
The title compound was prepared from (1S)-2-amino-1-[3-(3,4-dichloro-phenyl)isoxazol-5-yl]ethanol (which was obtained in Example 109) and 5-[4-(4-oxopiperidine-1-yl)benzyl]-1,3-thiazolidine-2,4-dione (which was obtained in Example 38) in substantially the same manner, as described in Example 106 and was obtained as a white solid (0.22 g, 48% yield), mp 110° C.; MS (ES) m/z: 561 (MH+); 1H NMR (400 MHz, DMSO-d6) δ 1.38 (m, 2H), 1.89 (m, 2H), 3.32-2.67 (m, 7H), 3.60 (m, 2H), 4.74 (m. 1H), 4.85 (m, 1H), 6.85 (d, 1H), 7.02 (d, 1H), 7.11 (s, 1H), 7.79 (d, 1H), 7.86 (d, 1H), 8.13 (s, 1H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06525202B2 |
| Source dataset | uspto-grants-2003_02 |
| ORD ID | ord-ec68cc95b39a4e0cb0a3153d2f90bd42 |
| Source note | uspto-grants-2003_02 |