HuagongsheHuagongshe Chemistry Print Report · For research reference only
1-(4-Aminophenyl)methanesulfonamide → HCID 10196752, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1-(4-Aminophenyl)methanesulfonamide | HCID 10821407 | — |
| Reactant | HCID 59674105 | HCID 59674105 | — |
| Product | HCID 10196752 | HCID 10196752 | — |
Reaction Steps
The title compound was prepared following the procedure of example one with N5-(2-chloro-pyrimidin-4-yl)-N2-(2-fluoro-benzyl)-1,N5-dimethyl-1H-benzoimidazole-2,5-diamine (60 mg, 0.15 mmol) and (4-amino-phenyl)-methanesulfonamide (28 mg, 0.15 mmol) as a white solid (30 mg, 34%). 1H NMR (300 MHz, d6-DMSO+NaHCO3) δ 9.58 (s, 1H), 7.83 (d, J=6.3 Hz, 1H), 7.68 (d, J=8.4 Hz, 2H), 7.49-7.53 (m, 2H), 7.33-7.40 (m, 1H), 7.17-7.27 (m, 4H), 7.09-7.12 (m, 1H), 6.79 (s, 2H), 5.76 (d, J=6.0 Hz, 1H), 4.72 (d, J=5.4 Hz, 2H), 4.18 (s, 2H), 3.67 (s, 3H), 3.46 (s, 3H). MS (ESI) m/z=547 [M+H]+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07338959B2 |
| Source dataset | uspto-grants-2008_03 |
| ORD ID | ord-c028f39c14df424b87dc21d431d775fa |
| Source note | uspto-grants-2008_03 |