HuagongsheHuagongshe Chemistry Print Report · For research reference only
Isatin → HCID 178444720, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Isatin | HCID 7054 | — |
| Reactant | adamantane-1-carbohydrazide | HCID 337203 | — |
| Product | HCID 178444720 | HCID 178444720 | 59% |
Reaction Steps
The title compound was prepared as a yellow solid, using isatin 3 and adamantanecarbohydrazide according to the synthetic method E. The resulting solid was washed with ethanol. Yield: 59%. 1H NMR (DMSO-d6): δ 0.85 (t, J=6.9 Hz, 3H), 1.27 (m, 6H), 1.60-1.65 (m, 2H), 1.72 (s, 6H), 1.91 (s, 6H), 2.05 (s, 3H), 3.75 (t, J=7.2 Hz, 2H), 7.16 (t, J=7.5 Hz, 1H), 7.21 (d, J=7.8 Hz, 1H), 7.46 (t, J=7.8 Hz, 1H), 7.59 (d, J=7.5 Hz, 1H), 13.28 (br s, 1H). 13C NMR (DMSO-d6): δ 14.32 (CH3), 22.44 (CH2), 26.38 (CH2), 27.41 (CH2), 27.85 (CH), 31.31 (CH2), 36.32 (CH), 38.80 (CH2), 39.52 (CH2), 110.59 (CH), 119.75 (C), 121.03 (CH), 123.61 (CH), 131.96 (CH), 143.27 (C═N), 161.39 (C═O). HRMS (ES+) calcd for C25H34N3O2 (M+H+), m/e, 408.2660; found, 408.2646.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08309595B2 |
| Source dataset | uspto-grants-2012_11 |
| ORD ID | ord-759dce12333144e8ab466be10ce6e329 |
| Source note | uspto-grants-2012_11 |