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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 594295Generated: October 26, 2026

Sodium borohydride → (2-(5-Methylthiazol-2-yl)pyridin-4-yl)methanol

https://huagongshe.com/reaction/594295

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
ReactantMethyl 2-(5-methylthiazol-2-yl)isonicotinateHCID 69082465—
SolventMethanolHCID 887—
Product(2-(5-Methylthiazol-2-yl)pyridin-4-yl)methanolHCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09242970B2
Source datasetuspto-grants-2016_01
ORD IDord-86bc52013600493b9105320c39b6a968
Source noteuspto-grants-2016_01