HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methylamine → 2',4'-Difluoro-N-(3-(2-hydroxy-1-(methylamino)ethyl)phenyl)biphenyl-4-sulfonamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methylamine | HCID 6329 | — |
| Reactant | 2',4'-Difluoro-N-(3-(oxiran-2-yl)phenyl)biphenyl-4-sulfonamide | HCID 86656262 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 2',4'-Difluoro-N-(3-(2-hydroxy-1-(methylamino)ethyl)phenyl)biphenyl-4-sulfonamide | HCID 67328738 | — |
Reaction Steps
Using a method analogous to Method D, using 2′,4′-difluoro-N-(3-(oxiran-2-yl)phenyl)biphenyl-4-sulfonamide and 33% methylamine in ethanol, the title compound was obtained as a light orange powder (165 mg) by flash chromatography of mixture of regioisomers which gave ABD783. 1H NMR (400 MHz, CDCl3): δ 2.10 (3H, s), 3.51 (1H, m), 3.60-3.62 (2H, m), 5.10 (3H, br s), 6.70-6.95 (3H, m), 7.10-7.15 (4H, m), 7.20-7.25 (1H, m), 7.34 (2H, d, J=8 Hz) and 7.73 (2H, d, J=8 Hz). MS, m/z: Calcd, 418.11. Found, 418.09 (M).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08207167B2 |
| Source dataset | uspto-grants-2012_06 |
| ORD ID | ord-e924b4bcaa5342a1ba20ae10a1d2584b |
| Source note | uspto-grants-2012_06 |