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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 538866Generated: October 31, 2026

Bromine → 6-(2-(dimethylamino)-1-(1H-imidazol-1-yl)butyl)benzo[d]thiazol-2-amine

https://huagongshe.com/reaction/538866

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBromineHCID 24408—
ReactantPotassium thiocyanateHCID 516872—
Reactant4-(2-(dimethylamino)-1-(1H-imidazol-1-yl)butyl)anilineHCID 86681895—
SolventAcetic AcidHCID 176—
Product6-(2-(dimethylamino)-1-(1H-imidazol-1-yl)butyl)benzo[d]thiazol-2-amineHCID 54759330—

Reaction Steps

Step-7: A solution of 4-(2-(dimethylamino)-1-(1H-imidazol-1-yl)butyl)aniline (600 mg, 2.32 mmol) and KSCN (508 mg, 5.22 mmol) in 15 mL AcOH was cooled to about 7° C. and treated with Br2 (125 μL, 2.43 mmol) in 2 mL AcOH added drop-wise via syringe over 5 min. The reaction vessel was removed from the cooling bath and stirred at rt for 1 hr. The reaction was cooled in an ice bath and basified with 3N NaOH (100 mL) added portionwise over several minutes. This mixture was then extracted with DCM (4×75 mL). The combined organic extracts were dried over Na2SO4, decanted and concentrated in vacuo. The residue was purified by silica gel column chromatography eluting with 6% MeOH (2N NH3)/DCM to give 6-(2-(dimethylamino)-1-(1H-imidazol-1-yl)butyl)benzo[d]thiazol-2-amine as a yellow foam. MS ESI: m/z 316.16 [M+1+].

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08865752B2
Source datasetuspto-grants-2014_10
ORD IDord-8ffccf12dbda434784c72b36f7b57182
Source noteuspto-grants-2014_10