HuagongsheHuagongshe Chemistry Print Report · For research reference only
N-[4-(4-fluoro-2-methoxyphenyl)pyridin-3-yl]-N-methyl-3-morpholin-4-ylsulfonyl-5-(trifluoromethyl)benzamide → N-[4-(4-Fluoro-2-methoxy-phenyl)-6-methyl-pyridin-3-yl]-N-methyl-3-(morpholine-4-sulfonyl)-5-trifluoromethyl-benzamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | N-[4-(4-fluoro-2-methoxyphenyl)pyridin-3-yl]-N-methyl-3-morpholin-4-ylsulfonyl-5-(trifluoromethyl)benzamide | HCID 60196904 | — |
| Reactant | 4-(4-fluoro-2-methoxyphenyl)-N,6-dimethylpyridin-3-amine | HCID 70663668 | — |
| Product | N-[4-(4-Fluoro-2-methoxy-phenyl)-6-methyl-pyridin-3-yl]-N-methyl-3-(morpholine-4-sulfonyl)-5-trifluoromethyl-benzamide | HCID 70663244 | — |
Reaction Steps
The title compound was prepared in analogy to example 90, from 4-(4-fluoro-2-methoxyphenyl)-N,6-dimethylpyridin-3-amine (example 301, intermediate a) and 3-(morpholinosulfonyl)-5-(trifluoromethyl)benzoic acid (example 256, intermediate) after a reaction time of 15.5 hours. The compound was purified by silica gel chromatography on a 20 g column using an MPLC system eluting with EtOAc (isocratic). The product was purified by preparative HPLC (Gemini NX column) using a gradient of MeOH:water (containing 0.1% formic acid) (20:80 to 98:2). Colorless oil (67%). MS (ESI): m/z=568.15 [M+H]+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08987307B2 |
| Source dataset | uspto-grants-2015_03 |
| ORD ID | ord-b5c35aeb07ab4e98b1e79fbde8b11f7a |
| Source note | uspto-grants-2015_03 |