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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 635842Generated: October 30, 2026

Sodium borohydride → HCID 467102, compound

https://huagongshe.com/reaction/635842

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
Reactant(2-Phenylethyl)-3-methylimidazo[2,1-b]thiazol-5-yl methanoneHCID 57013581—
SolventEthanolHCID 702—
ProductHCID 467102HCID 46710286.9%

Reaction Steps

A solution of (2-Phenylethyl)-3-methylimidazo[2,1-b]thiazol-5-yl methanone (Formula B-6) (0.40 g) in ethanol (5.0 mL) was treated with a solution of NaBH4 (0.05 g) in ethanol (5 mL) and reacted for 18 hours. The solvent was removed in vacuo and the residue was treated with 5% acetic acid solution. Precipitated 3-Methyl-α-(2-phenylethyl)imidazo[2,1-b]thiazole-5-methanol (Formula B-8) (0.38 g) was filtered and recrystallized from isopropanol solution to provide pure 3-Methyl-α-(2-phenylethyl)imidazo[2,1-b]thiazole-5-methanol (Formula B-8) (0.35 g), m.p. 144-145°.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06191124B1
Source datasetuspto-grants-2001_02
ORD IDord-c8d63c44a6bf4ce8afb4bd9c1c73bfbf
Source noteuspto-grants-2001_02