HuagongsheHuagongshe Chemistry Print Report · For research reference only
HCID 67083935, compound → HCID 67083714, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | HCID 67083935 | HCID 67083935 | — |
| Catalyst | Hydrochloric Acid | HCID 313 | — |
| Catalyst | HCID 178502593 | HCID 178502593 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 67083714 | HCID 67083714 | 77% |
Reaction Steps
A solution of 4-(2-fluoro-4-methylphenylamino)-7-methoxy-6-(1,2,3,6-tetrahydropyridin-4-yl)cinnoline-3-carboxamide (Example 52, 0.9 g, 2.21 mmol) in MeOH (44.2 ml) with a few drops of conc. HCl was passed through an H Cube apparatus using a 20 wt % Pd(OH)2/Carbon cartridge, at 10 bar. The solvent was removed under reduced pressure and the residue was purified with silica chromatography CH2Cl2/10% MeOH (1% NH4OH) to give 692 mg (77%) of a light yellow solid. 1H NMR: MeOD 7.61 (s, 1H), 7.37 (m, 1H), 7.23 (m, 1H), 7.12 (m, 2H), 4.09 (s, 3H), 3.38 (m, 2H), 3.22 (m, 1H), 3.12 (m, 2H), 2.43 (s, 3H), 1.90 (m, 2H), 1.36 (m, 2H); m/z 410.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07723337B2 |
| Source dataset | uspto-grants-2010_05 |
| ORD ID | ord-e4510d9e3cf94165b825cba51b900265 |
| Source note | uspto-grants-2010_05 |