HuagongsheHuagongshe Chemistry Print Report · For research reference only
1-(Bromomethyl)-4-(1,1-dimethylethyl)benzene → HCID 68987285, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1-(Bromomethyl)-4-(1,1-dimethylethyl)benzene | HCID 87836 | — |
| Reactant | N-Cyclopropyl-N-4-piperidinylbenzenesulfonamide | HCID 2735904 | — |
| Product | HCID 68987285 | HCID 68987285 | — |
Reaction Steps
Also, N-cyclopropyl-N-[1-(4-tert-butylbenzyl)piperidin-4-yl]-benzenesulfonamide was prepared from N-cyclopropyl-N-piperidin-4-yl-benzenesulfonamide and 1-bromomethyl-4-tert-butylbenzene. LC: 100%, MS: m/z=427.2, 428.3 (M+H+). 1H NMR (400 MHz, CDCl3): δ 7.85 (2H, m), 7.56 (1H, m), 7.50 (2H, m), 7.32 (2H, d, J=8.4 Hz), 7.19 (2H, d, J=8.4 Hz), 3.85 (1H, m), 3.44 (2H, s), 2.89 (1H, s), 2.87 (1H, s), 1.97 (5H, m), 1.59 (4H, s), 1.49 (1H, s), 1.47 (1H, s), 1.32 (9H, s), 0.97 (2H, m), 0.75 (2H, m).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09000174B2 |
| Source dataset | uspto-grants-2015_04 |
| ORD ID | ord-a1fd34d3d57b4726954ede6720d90bad |
| Source note | uspto-grants-2015_04 |