Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 514876Generated: October 31, 2026

Cyanogen Bromide → 4-(2-Aminobenzo[d]thiazole-4-sulfonamido)benzoic acid

https://huagongshe.com/reaction/514876

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCyanogen BromideHCID 10476—
Reactant4-(2-Amino-3-mercaptophenylsulfonamido)benzoic acidHCID 90419018—
SolventTetrahydrofuranHCID 8028—
Product4-(2-Aminobenzo[d]thiazole-4-sulfonamido)benzoic acidHCID 90419092100.9%

Reaction Conditions

Temperature80 °C

Reaction Steps

To a solution of 4-(2-amino-3-mercaptophenylsulfonamido)benzoic acid (671 mg, 2.07 mmol) in THF (15 mL) was added cyanic bromide (439.1 mg, 4.14 mmol) at r.t. The reaction mixture was stirred at 80° C. for 8 h. The resulting mixture was then cooled, and partitioned between water and EtOAc. The organic phase was washed with brine, dried over anhy. Na2SO4 and concentrated in vacuo to afford the title compound (730 mg). LC-MS: m/z 348.7 (M+H)+

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09108921B2
Source datasetuspto-grants-2015_08
ORD IDord-415e914287084f788a0b7290dcdf5e21
Source noteuspto-grants-2015_08