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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 908201Generated: October 27, 2026

Ethanol → [5-(3-Fluoro-4-methanesulfonyl-phenyl)-4-methyl-thiazol-2-yl]-(1H-pyrazol-3-yl)-amine

https://huagongshe.com/reaction/908201

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
ReactantBromineHCID 24408—
Reactant1-(3-Fluoro-4-(methylsulfonyl)phenyl)propan-2-oneHCID 57351278—
ReactantHCID 178514162HCID 178514162—
SolventChloroformHCID 6212—
Solvent1,4-DioxaneHCID 31275—
Product[5-(3-Fluoro-4-methanesulfonyl-phenyl)-4-methyl-thiazol-2-yl]-(1H-pyrazol-3-yl)-amineHCID 178433124—

Reaction Conditions

Temperature10 °C

Reaction Steps

1-(3-Fluoro-4-methanesulfonyl-phenyl)-propan-2-one (68c) (6.0 g, 26 mmol) is dissolved in dioxan (50 ml) and the solution is cooled to 10° C. at which point the mixture is semi frozen. A solution of bromine (0.9 ml, 17 mmol) in chloroform (2 ml) is added slowly over 30 minutes and the mixture is stirred for an additional 15 minutes in a semi frozen state. The mixture is then allowed to warm to room temperature and the solvent is removed to give a red oil. Ethanol (70 ml) and (1H-pyrazol-3-yl)-thiourea (35a) (3.2 g, 22 mmol) are added and the reaction is stirred at 60° C. for 30 minutes. The solution is allowed to cool to room temperature whereupon the product crystallises. Filtration affords the titled compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08017608B2
Source datasetuspto-grants-2011_09
ORD IDord-658e686f628d41828ce511394373a426
Source noteuspto-grants-2011_09