HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium borohydride → (2-(5-Methylthiazol-2-yl)pyridin-4-yl)methanol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | Methyl 2-(5-methylthiazol-2-yl)isonicotinate | HCID 69082465 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | (2-(5-Methylthiazol-2-yl)pyridin-4-yl)methanol | HCID 69084104 | — |
Reaction Steps
A solution of methyl 2-(5-methylthiazol-2-yl)isonicotinate (2.390 g; 10.20 mmol) in anh. MeOH (50 ml) was treated with NaBH4 (772 mg; 20.40 mmol), and the resulting mixture was stirred at rt, under nitrogen, for 24 h. After concentration to dryness under reduced pressure, the resulting residue was treated with water, and extracted with DCM. The organic layer was then dried over anh. MgSO4, filtered, and concentrated to dryness under reduced pressure. Purification by FC (DCM/MeOH=20/1) afforded (2-(5-methylthiazol-2-yl)pyridin-4-yl)methanol as an off-white solid. LC-MS (conditions A): tR=0.48 min.; [M+H]+: 207.05 g/mol.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09242970B2 |
| Source dataset | uspto-grants-2016_01 |
| ORD ID | ord-86bc52013600493b9105320c39b6a968 |
| Source note | uspto-grants-2016_01 |