HuagongsheHuagongshe Chemistry Print Report · For research reference only
HCID 23513780, compound → HCID 23513915, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | HCID 23513780 | HCID 23513780 | — |
| Reactant | HCID 86757881 | HCID 86757881 | — |
| Product | HCID 23513915 | HCID 23513915 | 43% |
Reaction Steps
Starting from 3-{[4-(2-butynyloxy)phenyl]sulfonyl}-1-(4-chlorobenzyl)-3-piperidinecarboxylic acid (1.1 g, 2.4 mmol) and and following the procedure as outlined in example 1, (step 8), 0.48 g of 3-{[4-(2-butynyloxy)phenyl]sulfonyl}-1-(4-chlorobenzyl)-3-N-hydroxy-3-piperidinecarboxamide hydrogen chloride was isolated as a white solid. Yield 43%; mp 124.4° C.; MS (ES): m/z: 477.1 (M+H)+; 1H NMR (300 MHz, DMSO-d6): δ2.0 (m, 2H), 3.39 (m, 5H), 4.27 (d, 2H), 4.89 (m, 2H), 7.14 (d, 2H), 7.15 (m, 4H), 7.61 (d, 2H), 8.95 (s, 1H), 9.46 (s, 1H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06753337B2 |
| Source dataset | uspto-grants-2004_06 |
| ORD ID | ord-48db68a1647645649a3bf245dae86b19 |
| Source note | uspto-grants-2004_06 |