Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2282297Generated: October 31, 2026

N-bromobutanimide → 2-Amino-4-(2,4-dichlorophenyl)thiazole-5-carbonitrile

https://huagongshe.com/reaction/2282297

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-bromobutanimideHCID 67184—
Reactantbeta-CyclodextrinHCID 444041—
ReactantThioureaHCID 2723790—
Reactant3-(2,4-Dichlorophenyl)-3-oxopropanenitrileHCID 13630728—
SolventAcetoneHCID 180—
SolventWaterHCID 962—
Product2-Amino-4-(2,4-dichlorophenyl)thiazole-5-carbonitrileHCID 5809521642%

Reaction Conditions

Temperature50 °C

Reaction Steps

beta-Cyclodextrin (4.29 g, 3.78 mmol) was dissolved in water (75 mL) at 50° C. and a solution of 3-(2,4-dichlorophenyl)-3-oxopropanenitrile (810 mg, 3.8 mmol) in Acetone (3.80 mL) was added dropwise, followed by NBS (0.808 g, 4.54 mmol) and thiourea (0.346 g, 4.54 mmol). Reaction mixture was stirred at 50° C. 1 hr. LCMS indicated complete conversion. Reaction mixture was cooled to rt, extracted with ethyl acetate (3×50 mL), dried with MgSO4, filtered and concentrated under reduced pressure. The residue was purified by ISCO with 5-30% ethyl acetate in hexanes to give 0.43 g of the title compound (42%). LCMS: (FA) ES+, 270, 272. 1H NMR (400 MHz, d1-chloroform) δ 7.49 (d, J=1.84 Hz, 1H), 7.41 (d, J=8.30 Hz, 1H), 7.31 (dd, J=8.16, 1.74 Hz, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09139589B2
Source datasetuspto-grants-2015_09
ORD IDord-bedf96aa40ba47c5934efe4577cb190b
Source noteuspto-grants-2015_09