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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 858983Generated: October 31, 2026

Sodium hydride → HCID 21865074, compound

https://huagongshe.com/reaction/858983

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium hydrideHCID 24758—
Reactant2-Methyl-1,3-benzothiazol-5-olHCID 699799—
ReactantHCID 16749212HCID 16749212—
SolventDimethylformamideHCID 6228—
ProductHCID 21865074HCID 21865074—

Reaction Steps

To a 100-mL, round-bottomed flask containing 4-(4-tert-butyl-phenyl)-6-chloro-pyrimidine, (Example 1(a)), (0.15 g, 0.61 mmol) and 2-methyl-benzothiazol-5-ol (0.14 g, 0.85 mmol, Aldrich) in DMF (10 mL), was added NaH (34 mg, 0.85 mmol, 60% in mineral oil, Aldrich) at room temperature. The solution was then stirred at room temperature for 4 h. After the solvent was removed in vacuum, EtOAc (10 mL) was added to the residue, and the organic layer was washed with water (8 mL), dried over Na2SO4, filtered, and concentrated in vacuum. After purifying the crude product by silica gel chromatography (4:1 hexanes/EtOAc), the resulting solid was dissolved in acetone (5 mL). Water (8 mL) was added dropwise to this mixture, and a white precipitate fell out of solution, which was collected by filtration, washed with water (0.5 mL), and dried under vacuum at 50° C. for 48 h to furnish the title compound. Mp: 163–165° C. MS (ESI, pos. ion) m/z: 376 (M+1). Anal. Calcd for C23H21N3OS.(H2O)1/3: C, 69.26; H, 5.72; N, 11.01. Found: C, 69.19; H, 5.61; N, 11.03.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07148221B2
Source datasetuspto-grants-2006_12
ORD IDord-cb7891c8aa4140d88f46b1a17ab0a0ee
Source noteuspto-grants-2006_12