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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 538886Generated: October 31, 2026

Ammonium Hydroxide → 6-(2-ethyl-1-(1H-imidazol-1-yl)butyl)benzo[d]thiazol-2-amine

https://huagongshe.com/reaction/538886

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium HydroxideHCID 14923—
ReactantBromineHCID 24408—
ReactantPotassium thiocyanateHCID 516872—
Reactant4-(2-ethyl-1-(1H-imidazol-1-yl)butyl)anilineHCID 86681897—
SolventAcetic AcidHCID 176—
Product6-(2-ethyl-1-(1H-imidazol-1-yl)butyl)benzo[d]thiazol-2-amineHCID 54759531—

Reaction Steps

A solution of 4-(2-ethyl-1-(1H-imidazol-1-yl)butyl)aniline (285 mg, 1.17 mmol) and KSCN (455 rug, 4.68 mmol) in AcOH (6 mL) was stirred until all dissolved at RT and then treated with Br2 (0.063 mL, 1.23 mmol) in AcOH (2 mL) added drop wise via syringe over 5 min. The reaction mixture was stirred overnight at RT. The reaction mixture was diluted with ice water and then basified with NH4OH (pH 12). The aqueous phase was extracted three times with DCM and the organic extracts were combined and dried over filtered and then concentrated. The crude product was purified by preparative TLC using 5% MeOH in DCM as eluent to afford to 6-(2-ethyl-1-(1H-imidazol-1-yl)butyl)benzo[d]thiazol-2-amine as pale yellow solid. MS (ES+): 301.27 (MH+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08865752B2
Source datasetuspto-grants-2014_10
ORD IDord-cd7b110de2144c1796a2e9bcad9a8cd1
Source noteuspto-grants-2014_10