HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dimethylamine → N-(3-(1-(Dimethylamino)-2-hydroxyethyl)phenyl)-2',4'-difluorobiphenyl-4-sulfonamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dimethylamine | HCID 674 | — |
| Reactant | 2',4'-Difluoro-N-(3-(oxiran-2-yl)phenyl)biphenyl-4-sulfonamide | HCID 86656262 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | N-(3-(1-(Dimethylamino)-2-hydroxyethyl)phenyl)-2',4'-difluorobiphenyl-4-sulfonamide | HCID 45138189 | — |
Reaction Steps
Using a method analogous to Method D, using 2′,4′-difluoro-N-(3-(oxiran-2-yl)phenyl)biphenyl-4-sulfonamide and 33% dimethylamine in ethanol, a mixture of regioisomers was obtained. Reverse-phase HPLC was used to purify the mixture and the title compound was obtained as a pale orange powder from the mixture of isomers as gave ABD784. 1H NMR (300 MHz, CDCl3): δ 2.08 (6H, s), 3.40 (3H, m), 3.48 (1H, m), 3.62-3.64 (1H, m), 6.87-6.96 (3H, m), 7.04-7.12 (2H, m), 7.20-7.25 (1H, m), 7.33-7.40 (1H, m), 7.53 (2H, d, J=8 Hz) and 7.78 (2H, d, J=8 Hz). MS, m/z: Calcd, 432.132. Found, 432.56 (M).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08207167B2 |
| Source dataset | uspto-grants-2012_06 |
| ORD ID | ord-8e5b537ffdef485591e1b715044ad490 |
| Source note | uspto-grants-2012_06 |