HuagongsheHuagongshe Chemistry Print Report · For research reference only
HCID 10112187, compound → HCID 10203688, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | HCID 10112187 | HCID 10112187 | — |
| Reactant | HCID 22634064 | HCID 22634064 | — |
| Product | HCID 10203688 | HCID 10203688 | 26% |
Reaction Steps
Starting from a mixture of 2{[4-(2-butynyloxy)phenyl]sulfanyl}-N-hydroxy-2-[4-(2-thienyl)phenyl]acetamide and 2-{[4-(2-butynyloxy)phenyl]sulfinyl}-N-hydroxy-2-[4-(2-thienyl)phenyl]ethanamide (410 mg, 0.96 mmol), and following the procedure as outlined in Example 75, 110 mg of 2-{[4-(2-butynyloxy)phenyl]sulfonyl}-N-hydroxy-2-[4-(2-thienyl)phenyl]acetamide was isolated as a gray solid. mp: 175° C.; Yield: 26%; MS: 442.2 (M+W)+; 1H NMR (300 MHz, DMSO-d6): δ 1.83 (t, 3H), 4.85 (d, J=2.01 Hz, 2H), 5.04 (s, 1H), 7.11 (m, 4H), 7.39 (d, 7.49-7.63 (band, 5H), 9.30 (s, 1H), 10.9 (s, 1H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06825354B2 |
| Source dataset | uspto-grants-2004_11 |
| ORD ID | ord-13414f2bbd1c42fda4a782679a5bf678 |
| Source note | uspto-grants-2004_11 |