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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 347408Generated: October 29, 2026

Water → 1-(4-Bromo-1,3-thiazol-2-YL)piperidine

https://huagongshe.com/reaction/347408

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactant2,4-Dibromo-1,3-thiazoleHCID 2763297—
Reactant2-Piperidinyl(trimethylstannyl)thiazoleHCID 59118286—
SolventPiperidineHCID 8082—
Product1-(4-Bromo-1,3-thiazol-2-YL)piperidineHCID 45787499100%

Reaction Conditions

Temperature50 °C

Reaction Steps

Synthesis of 2-Piperidinyl(trimethylstannyl)thiazole 373 as illustrated in FIG. 53. 2,4-Dibromothiazole (358; 1.0 equiv) was dissolved in piperidine (0.5 M) and the reaction was warmed to 50° C. for 8 h, upon which completion of the reaction was indicated by TLC. The mixture was poured into water and extracted with ether (2×). Drying (MgSO4) and evaporation of the solvents gave 2-piperidinyl-4-bromothiazole 372, which was isolated after flash column chromatography (silica gel, 5% EtOAc in hexanes) in 100% yield.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07173137B2
Source datasetuspto-grants-2007_02
ORD IDord-63123ab641a34326bbff78639f93cc89
Source noteuspto-grants-2007_02