Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 389480Generated: October 31, 2026

N-bromobutanimide → 7-Bromo-1,2,3-benzothiadiazol-4-amine

https://huagongshe.com/reaction/389480

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-bromobutanimideHCID 67184—
Reactantbenzo[d][1,2,3]thiadiazol-4-aMineHCID 21936630—
SolventTetrahydrofuranHCID 8028—
Product7-Bromo-1,2,3-benzothiadiazol-4-amineHCID 6676043730%

Reaction Steps

A mixture of 1,2,3-benzothiadiazol-4-amine (200.0 mg, 1.323 mmol) and NBS (341.4 mg, 1.918 mmol) in THF (10 mL) was stirred at RT overnight. The solution was adsorbed onto silica gel and purified by ISCO chromatography (10 to 30% EtOAc:heptane) to afford 80 mg (30%) of the title compound as a yellow solid. 1H NMR (400 MHz, DMSO-d6): δ 6.74 (d, J=8.3 Hz, 1 H), 6.97 (s, 2 H), 7.60 (d, J=8.3 Hz, 1 H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08378104B2
Source datasetuspto-grants-2013_02
ORD IDord-4b16701705834caabacd0ca970e00cf2
Source noteuspto-grants-2013_02