HuagongsheHuagongshe Chemistry Print Report · For research reference only
Veratrylamine → 5-(benzyloxy)-N-(3,4-dimethoxybenzyl)-4-fluoro-2-(tetrahydro-2H-pyran-4-ylamino)benzamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Veratrylamine | HCID 79832 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | Methanaminium, N-((1H-benzotriazol-1-yloxy)(dimethylamino)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1) | HCID 2733084 | — |
| Reactant | 5-(benzyloxy)-4-fluoro-2-(tetrahydro-2H-pyran-4-ylamino)benzoic acid | HCID 66732719 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 5-(benzyloxy)-N-(3,4-dimethoxybenzyl)-4-fluoro-2-(tetrahydro-2H-pyran-4-ylamino)benzamide | HCID 67496404 | 79.8% |
Reaction Steps
A mixture of 14 g of the compound obtained in Step 4.4, 7.46 g of veratrylamine, 19.99 g of HBTU and 13.1 g of DIEA in 300 ml of DMF is stirred for 2 hours at room temperature. The solvent is evaporated off under reduced pressure and the residue is taken up in DCM. The resulting solution is washed twice with saturated aqueous NaHCO3 solution. The organic phase is dried over Na2SO4 and filtered, and the filtrate is evaporated under reduced pressure. The residue is chromatographed on silica gel, eluting with a PE/EtOAc mixture from (90/10, v/v) to (40/60, v/v) to give 16 g of the expected product.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08722659B2 |
| Source dataset | uspto-grants-2014_05 |
| ORD ID | ord-12e99084da394e919e3ec3a97e0bd5ad |
| Source note | uspto-grants-2014_05 |