HuagongsheHuagongshe Chemistry Print Report · For research reference only
Isatin → HCID 178444727, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Isatin | HCID 7054 | — |
| Reactant | 4-Chlorobenzohydrazide | HCID 10816 | — |
| Product | HCID 178444727 | HCID 178444727 | 80% |
Reaction Steps
The title compound was prepared as a yellow solid, using isatin 3 and 4-chlorobenzhydrazide according to the synthetic method E. The resulting solid was washed with ethanol. Yield: 80%. 1H NMR (DMSO-d6): δ 0.85 (t, J=6.9 Hz, 3H), 1.25-1.38 (m, 6H), 1.64 (m, 2H), 3.76 (t, J=7.2 Hz, 2H), 7.18 (t, J=7.8 Hz, 1H), 7.23 (d, J=7.8 Hz, 1H), 7.48 (t, J=7.8 Hz, 1H), 7.64-7.72 (m, 3H), 7.91-7.94 (m, 2H), 13.85 (br s, 1H). 13C NMR (DMSO-d6): δ 14.32 (CH3), 22.41 (CH2), 26.37 (CH2), 27.38 (CH2), 31.31 (CH2), 39.80 (CH2), 110.69 (CH), 119.56 (C), 121.33 (CH), 123.72 (CH), 129.75 (CH), 131.20 (C), 132.35 (CH), 138.23 (C), 143.52 (C═N), 161.55 (C═O). HRMS (ES+) calcd for C21H23N3O2Cl (M+H+), m/e, 384.1484; found, 384.1473.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08309595B2 |
| Source dataset | uspto-grants-2012_11 |
| ORD ID | ord-0e1d581c4da1444bbf03689a99cd60a3 |
| Source note | uspto-grants-2012_11 |