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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1529564Generated: November 2, 2026

Sodium borohydride → HCID 66608179, compound

https://huagongshe.com/reaction/1529564

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 66609439HCID 66609439—
SolventMethanolHCID 887—
SolventWaterHCID 962—
ProductHCID 66608179HCID 6660817979%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09090632B2
Source datasetuspto-grants-2015_07
ORD IDord-7e59977795e34e0e9617a56fbff12ae7
Source noteuspto-grants-2015_07