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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2196192Generated: October 29, 2026

N-bromobutanimide → 4-Bromo-1,3-benzothiazol-5-amine

https://huagongshe.com/reaction/2196192

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-bromobutanimideHCID 67184—
ReactantBenzothiazol-5-amineHCID 70749—
SolventAcetonitrileHCID 6342—
Product4-Bromo-1,3-benzothiazol-5-amineHCID 2246222386.6%

Reaction Steps

A stirred solution of 3 g of 5-aminobenzothiazole in 100 ml of acetonitrile at room temperature was treated with 3.5 g of N-bromosuccinimide and the resulting solution was stirred at room temperature for 4 hours. The solvent was removed under reduced pressure and the residue purified by silica gel chromatography (eluent cyclohexane/ethyl acetate 7:3) to afford 3.9 g of 5-amino-4-bromobenzothiazole as a pink solid. MS (ES+) 229/231 (MH+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08338443B2
Source datasetuspto-grants-2012_12
ORD IDord-acd3c265866944a19ce987aa0fab50dc
Source noteuspto-grants-2012_12