HuagongsheHuagongshe Chemistry Print Report · For research reference only
Isatin → HCID 178448701, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Isatin | HCID 7054 | — |
| Reactant | Benzoylhydrazine | HCID 11955 | — |
| Product | HCID 178448701 | HCID 178448701 | 65.3% |
Reaction Steps
The title compound was prepared as a yellow solid, using isatin 5 and benzhydrazide according to the synthetic method D. The resulting solid was washed with ethanol. Yield: 65.3%. 1H NMR (DMSO-d6): δ 0.95 (t, J=7.5 Hz, 3H), 1.36-1.41 (m, 2H), 1.64-1.69 (m, 2H), 3.78 (t, J=7.2 Hz, 2H), 7.19 (t, Hz, J=7.5 Hz, 1H), 7.24 (d, J=7.8 Hz, 1H), 7.49 (td, J=1.2 Hz, J=7.8 Hz, 1H), 7.60-7.73 (m, 4H), 7.90-7.92 (m, 2H), 13.90 (br, s 1H). 13C NMR (DMSO-d6): δ 14.06 (CH3), 20.04 (CH2), 29.56 (CH2), 39.49 (CH2), 110.69 (CH), 119.66 (C), 121.26 (CH), 123.69 (CH), 127.88 (CH), 129.67 (CH), 132.22 (CH), 132.43 (C), 133.40 (CH), 137.40 (C), 143.43 (C═N), 161.58 (C═O), 163.34 (C═O). HRMS (ES+) calcd for C19H20N3O2 (M+H+), m/e, 322.1548; found, 322.1550.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08309595B2 |
| Source dataset | uspto-grants-2012_11 |
| ORD ID | ord-9951c0ee73714dc483e12d30335b32f6 |
| Source note | uspto-grants-2012_11 |