HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium borohydride → HCID 66608179, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | HCID 66609439 | HCID 66609439 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 66608179 | HCID 66608179 | 79% |
Reaction Steps
Sodium borohydride (0.035 g, 0.94 mmol) was added to a stirred suspension of 5-(2-fluorobenzoyl)-4,5,6,7-tetrahydro-thiazolo[5,4-c]pyridine-2-carboxylic acid methyl ester (0.25 g, 0.78 mmol) in MeOH (5 mL). The mixture was stirred at room temperature for 3 hours, diluted with H2O and extracted with AcOEt. The organic layer was separated, dried (Na2SO4), filtered and the solvent evaporated in vacuo. The crude product was purified by preparative TLC (AcOEt in petroleum ether 50/50) to yield 5-(2-fluorobenzoyl)-4,5,6,7-tetrahydro-thiazolo[5,4-c]pyridine-2-methanol (0.18 g, 79% yield).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09090632B2 |
| Source dataset | uspto-grants-2015_07 |
| ORD ID | ord-7e59977795e34e0e9617a56fbff12ae7 |
| Source note | uspto-grants-2015_07 |