HuagongsheHuagongshe Chemistry Print Report · For research reference only
5-tert-butyl-2,3-dihydro-1H-inden-1-amine → N-(5-tert-butyl-2,3-dihydro-1H-inden-1-yl)-N'-5-isoquinolinylurea
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 5-tert-butyl-2,3-dihydro-1H-inden-1-amine | HCID 11506601 | — |
| Reactant | 5-Isocyanatoisoquinoline | HCID 11586357 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | N-(5-tert-butyl-2,3-dihydro-1H-inden-1-yl)-N'-5-isoquinolinylurea | HCID 11485180 | — |
Reaction Steps
5-tert-Butyl-2,3-dihydro-1H-inden-1-ylamine (150 mg, 1.13 mmol) in diethyl ether (10 mL) was treated with 5-isocyanatoisoquinoline in diethyl ether. The mixture was stirred for 2 hours, filtered, and the filter cake was washed with diethyl ether to provide the title compound. NMR (DMSO-d6) 1.29 (s, 9H), 1.78-1.90 (m, 1H), 2.43-2.54 (m, 1H, buried under DMSO), 2.76-3.05 (m, 2H), 5.19 (m, 1H), 7.27 (m, 2H), 7.31 (m, 1H), 7.43 (d, 1H), 7.89 (t, 1H), 8.05 (d, 1H), 8.63 (d, 1H), 8.69 (d, 1H), 9.33 (s, 1H), 9.73 (s, 1H); MS (ESI+) 360 (M+H)+; Elemental: Calculated for C23H25N3O.HCl.0.5H2O: C68.22, H6.72, N10.38; Found: C68.31, H6.81, N10.16.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08487116B2 |
| Source dataset | uspto-grants-2013_07 |
| ORD ID | ord-6567957418d24a848087d64fdc8ec070 |
| Source note | uspto-grants-2013_07 |