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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1851791Generated: October 31, 2026

Imidazole → N-Methyl-2-(6-methylaminopyridin-3-yl)benzothiazol-6-amine

https://huagongshe.com/reaction/1851791

Reaction equation

Participants

RoleNameHCIDCharge
ReactantImidazoleHCID 795—
ReactantDimethylformamideHCID 6228—
Reactanttert-Butyldimethylsilyl chlorideHCID 28928—
Reactant2-Amino-6-benzothiazololHCID 33462—
ProductN-Methyl-2-(6-methylaminopyridin-3-yl)benzothiazol-6-amineHCID 24804556—

Reaction Steps

A solution of 2-amino-6-hydroxybenzothiazole (5.00 g, 30.1 mmol), TBDMSCl (5.40 g, 1.2 equiv) and imidazole (2.46 g, 1.2 equiv) in DMF (160 ml) was stirred at ambient temperature for 16 h. The reaction mixture was then partitioned between water and ethyl acetate. The aqueous phase was extracted twice with ethyl acetate and the combined organics dried (MgSO4) and concentrated in vacuo. The crude product thus obtained was purified by silica gel chromatography by gradient elution (n-heptane:ethyl acetate) to yield 3.0 g of the title compound as a yellowish solid. 1H NMR δ 7.23 (br s, 2H) 7.18 (d, 1H) 7.16 (d, 1H) 6.70 (dd, 1H) 0.95 (s, 9H) 0.16 (s, 6 H); MS m/z (M+H) 281.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08957215B2
Source datasetuspto-grants-2015_02
ORD IDord-f1744473e3984aa49fa21da7790efa57
Source noteuspto-grants-2015_02