HuagongsheHuagongshe Chemistry Print Report · For research reference only
HCID 22915463, compound → HCID 22915451, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | HCID 22915463 | HCID 22915463 | — |
| Reactant | HCID 22915464 | HCID 22915464 | — |
| Product | HCID 22915451 | HCID 22915451 | — |
Reaction Steps
The desired compound was prepared according to the method of Example 15, step 4, except substituting O-benzyl-4-[3-(4-cyanophenyl)phenoxy]butanohydroxamic acid, prepared as in step 1, for N-benzyloxy-4-[3-(4-fluorophenyl)phenoxy]butyramide. 1H NMR (DMSO-d6) δ 1.97 (m, 2H), 2.15 (t, 2H, J=7.3 Hz), 4.05 (t, 2H, J=6.2 Hz), 7.01 (m, 1H), 7.29 (m, 2H), 7.42 (t, 1H, J=8.1 Hz), 7.91 (m, 4H), 8.72 (s, 1H), 10.42 (s, 1H). MS (FAB(+)) 297 (M+H+, 95), 264 (80), 102 (100); (FAB(-)) 295 (M-H-, 20), 194 (100). Anal. Calcd for C17H16N3O3 : C, 68.91; H, 5.44; N, 9.45. Found: C, 57.96; H, 4.66; N, 7.41.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05665777 |
| Source dataset | uspto-grants-1997_09 |
| ORD ID | ord-ff55ca97e23a4bb3953be27144dae67e |
| Source note | uspto-grants-1997_09 |