HuagongsheHuagongshe Chemistry Print Report · For research reference only
1-(4-Aminophenyl)methanesulfonamide → HCID 10240062, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1-(4-Aminophenyl)methanesulfonamide | HCID 10821407 | — |
| Reactant | HCID 59674100 | HCID 59674100 | — |
| Product | HCID 10240062 | HCID 10240062 | — |
Reaction Steps
The title compound was prepared following the procedure of example one with N2-(4-Chloro-benzyl)-N5-(2-chloro-pyrimidin-4-yl)-1,N5-dimethyl-1H-benzoimidazole-2,5-diamine (103 mg, 0.25 mmol) and (4-amino-phenyl)-methanesulfonamide (46 mg, 0.25 mmol) as a white solid (90 mg, 60%). 1H NMR (300 MHz, d6-DMSO+NaHCO3) δ 9.31 (s, 1H), 8.05 (br s, 1H), 7.72-7.80 (m, 3H), 7.46 (d, J=8.4 Hz, 2H), 7.38 (d, J=8.4 Hz, 2H), 7.32 (d, J=8.4 Hz, 1H), 7.20 (d, J=8.4 Hz, 2H), 7.14 (s, 1H), 6.93 (d, J=8.4 Hz, 1H), 6.78 (s, 2H), 5.66 (d, J=6.0H, 1H), 4.62 (d, J=5.4 Hz, 2H), 4.17 (s, 2H), 3.63 (s, 3H), 3.44 (s, 3H). MS (ESI) m/z=563 [M+H]+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07338959B2 |
| Source dataset | uspto-grants-2008_03 |
| ORD ID | ord-dc999a90d3bc4906a492eec5a1d46267 |
| Source note | uspto-grants-2008_03 |