HuagongsheHuagongshe Chemistry Print Report · For research reference only
(2-Methoxy-4-(trifluoromethyl)phenyl)boronic acid → HCID 86687515, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | (2-Methoxy-4-(trifluoromethyl)phenyl)boronic acid | HCID 24901776 | — |
| Reactant | HCID 86687516 | HCID 86687516 | — |
| Product | HCID 86687515 | HCID 86687515 | — |
Reaction Steps
The title compound was prepared in an analogous manner to that of Example 228, except that 1-chloro-4-cyano-N-(4-methoxybenzyl)-N-(pyrimidin-4-yl)isoquinoline-6-sulfonamide and (2-methoxy-4-(trifluoromethyl)phenyl)boronic acid were used as the coupling partners. The final compound was purified via column chromatography (12 g silica gel column, gradient elution 50 to 100% EtOAc:Heptane) to afford 4-cyano-1-(2-methoxy-4-(trifluoromethyl)phenyl)-N-(pyrimidin-4-yl)isoquinoline-6-sulfonamide as a white solid. 1H NMR (400 MHz, DMSO-d6) δ ppm=9.30 (s, 1H), 8.68-8.51 (m, 2H), 8.14 (d, J=9.6 Hz, 1H), 7.91 (d, J=8.7 Hz, 1H), 7.67-7.60 (m, 1H), 7.59-7.49 (m, 2H), 3.76 (s, 3H). m/z (ESI) 486.2 (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09012443B2 |
| Source dataset | uspto-grants-2015_04 |
| ORD ID | ord-2df2f50cb00847da8f4602c2ee39b9b6 |
| Source note | uspto-grants-2015_04 |