HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hexane → N-(3,4-dichlorobenzyl)-N'-1H-indol-4-ylurea
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hexane | HCID 8058 | — |
| Reactant | 4-Aminoindole | HCID 583431 | — |
| Reactant | 1,2-Dichloro-4-(isocyanatomethyl)benzene | HCID 2733368 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | N-(3,4-dichlorobenzyl)-N'-1H-indol-4-ylurea | HCID 10042481 | — |
Reaction Steps
4-Aminoindole (0.13 g, 1 mmol) in THF (3 mL) was treated with 1,2-dichloro-4-(isocyanatomethyl)benzene (0.22 g, 1.1 mmol) for 3 h at ambient temperature. Hexane was added to the reaction mixture to precipitate 0.25 g of the title compound as a tan solid. mp 201° C.; 1H NMR (300 MHz, DMSO-d6) δ 4.23 (d, 2H), 6.36 (s, 1H), 6.54 (t, 1H), 7.0 (dd, 1H), 7.25 (m, 2H), 7.30 (d, 2H), 7.45 (d, 1H), 7.6 (m, 2H), 8.31 (s, 1H), 10.87 (s, 1H) MS (DCI+) m/z 336 (M+H); Anal. Calcd. For C16H13N3Cl2O: C, 57.50; H, 3.92; N, 12.57. Found: C, 56.94, H, 3.68; N, 11.97.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06933311B2 |
| Source dataset | uspto-grants-2005_08 |
| ORD ID | ord-f54100d90f1b4f75a88a126f3cd500e4 |
| Source note | uspto-grants-2005_08 |