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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1890555Generated: November 1, 2026

Sodium borohydride → Thiazolo[4,5-c]pyridin-2-ylmethanol

https://huagongshe.com/reaction/1890555

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
ReactantEthyl thiazolo[4,5-c]pyridine-2-carboxylateHCID 65583458—
SolventEthanolHCID 702—
ProductThiazolo[4,5-c]pyridin-2-ylmethanolHCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08507487B2
Source datasetuspto-grants-2013_08
ORD IDord-d897d3a298544ca19178d3db356dce84
Source noteuspto-grants-2013_08