HuagongsheHuagongshe Chemistry Print Report · For research reference only
(2-Methylpyridin-4-yl)methanol → 2,6-Difluoro-3-[(2-methyl-4-pyridinyl)methoxy]benzenecarboxamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | (2-Methylpyridin-4-yl)methanol | HCID 9942144 | — |
| Reactant | 2,6-Difluoro-3-hydroxybenzamide | HCID 45120136 | — |
| Product | 2,6-Difluoro-3-[(2-methyl-4-pyridinyl)methoxy]benzenecarboxamide | HCID 59402990 | 34% |
Reaction Steps
Synthesised from 2,6-difluoro-3-hydroxybenzenecarboxamide according to Method C, scheme 3. The required building block, 4-hydroxymethyl-2-methylpyridine, was synthesised according to the literature method, shown in Scheme 23 (Ragan, J. A., Jones, B. P., Meltz, C. N., Teixeira J. J. Jr.; Synthesis 2002, 483-486. Yield 34%, mp 185-186° C., HPLC-MS (method 1): m/z 279 [M+H]+, Rt=2.50 min.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08088791B2 |
| Source dataset | uspto-grants-2012_01 |
| ORD ID | ord-5ee878e59a1c44468ad7e53d661af8aa |
| Source note | uspto-grants-2012_01 |