HuagongsheHuagongshe Chemistry Print Report · For research reference only
HCID 178442072, compound → HCID 178442074, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | HCID 178442072 | HCID 178442072 | — |
| Reactant | HCID 178442073 | HCID 178442073 | — |
| Product | HCID 178442074 | HCID 178442074 | 79% |
Reaction Steps
Reduction of the mixture of 4-{N′-[4-(2-methyl-1-butenyl)-2-oxo-1,2-dihydro-indol-3-ylidene]-hydrazino}-benzenesulfonamide and 4-{N′-[4-(2-methyl-2-butenyl)-2-oxo-1,2-dihydro-indol-3-ylidene]-hydrazino}benzenesulfonamide according to Procedure M gave the title compound in 79% yield: 1H NMR (DMSO-d6): δ 0.87-0.90 (m, 6H), 1.21-1.25 (m, 2H), 1.47-1.63 (m, 1H), 2.82 (dd, J=12.6, 8.1 Hz, 1H), 2.95 (dd, J=12.6, 6.6 Hz, 1H), 6.77 (d, J=7.7 Hz, 1H), 6.84 (d, J=7.7 Hz, 1H), 7.18 (t, J=7.7 Hz, 1H), 7.25 (s, 2H), 7.49 (d, J=8.6 Hz, 2H), 7.79 (d, J=8.6 Hz, 2H), 11.12 (s, 1H), 13.04 (s, 1H); APCI−MS m/z 385 (M−1)−.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06387919B1 |
| Source dataset | uspto-grants-2002_05 |
| ORD ID | ord-fa4eede336ff498e8efca199d4ff94a1 |
| Source note | uspto-grants-2002_05 |