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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 447015Generated: October 29, 2026

Ammonia → 7-Bromo-5-pyrazol-1-yl-benzothiazol-2-ylamine

https://huagongshe.com/reaction/447015

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmoniaHCID 222—
ReactantBromineHCID 24408—
Reactant(3-Bromo-5-pyrazol-1-yl-phenyl)-thioureaHCID 57813577—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
Product7-Bromo-5-pyrazol-1-yl-benzothiazol-2-ylamineHCID 5781369733.9%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution of (3-bromo-5-pyrazol-1-yl-phenyl)-thiourea (1.0 g, 3.0 mmol) in DCM (17.0 mL) at 0° C. was added dropwise a solution of Br2 (1.07 g, 6.0 mmol, in 3.0 ml of DCM) over a period of 15 min. The reaction mixture was stirred at 0° C. for 15 min followed by refluxing for 2 h. The reaction mixture was cooled to room temperature and filtered to get the crude residue that was washed with hexane and diethyl ether. The solid thus obtained was dissolved in H2O, basified with aqueous ammonia solution to pH 10-12 and extracted with ethyl acetate (×3). The combined organic was washed with water, dried (Na2SO4), filtered and concentrated. The residue was purified over silica gel (230-400 M, 25% EtOAc-Hexane) to get the desired product (0.30 g, 30%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08481544B2
Source datasetuspto-grants-2013_07
ORD IDord-11fe587a16654129a22189c79c234f8e
Source noteuspto-grants-2013_07