HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium borohydride → Thiazolo[4,5-c]pyridin-2-ylmethanol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | Ethyl thiazolo[4,5-c]pyridine-2-carboxylate | HCID 65583458 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | Thiazolo[4,5-c]pyridin-2-ylmethanol | HCID 55296405 | — |
Reaction Steps
To a solution of ethyl thiazolo[4,5-c]pyridine-2-carboxylate (R-3) (5 g, 24 mmol) in ethanol (100 mL) was added NaBH4 (0.9 g, 24 mmol) in portions at 0° C. The suspension was stirred at room temperature for 1 h, and then concentrated. The resulting residue was dissolved in EtOAc, washed with water. The organic layer was separated, dried over Na2SO4, concentrated in vacuo and purified by chromatography on silica gel to give the title compound. MS (m/z): 167 (M+1)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08987269B2 |
| Source dataset | uspto-grants-2015_03 |
| ORD ID | ord-0e902d08eb0543d48737ba84b67a22d6 |
| Source note | uspto-grants-2015_03 |