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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1426530Generated: November 1, 2026

Thiazole → 4-(1,3-thiazol-5-yl)-7-[2-(trimethylsilyl)ethoxy]methyl-7H-pyrrolo[2,3-d]pyrimidine

https://huagongshe.com/reaction/1426530

Reaction equation

Participants

RoleNameHCIDCharge
ReactantThiazoleHCID 9256—
ReactantPotassium AcetateHCID 517044—
Reactant4-Chloro-7-((2-(trimethylsilyl)ethoxy)methyl)-7H-pyrrolo(2,3-d)pyrimidineHCID 46736797—
CatalystHCID 178418397HCID 178418397—
SolventDimethylacetamideHCID 31374—
Product4-(1,3-thiazol-5-yl)-7-[2-(trimethylsilyl)ethoxy]methyl-7H-pyrrolo[2,3-d]pyrimidineHCID 5747762064%

Reaction Conditions

Temperature200 °C

Reaction Steps

4-Chloro-7-[2-(trimethylsilyl)ethoxy]methyl-7H-pyrrolo[2,3-d]pyrimidine (3.00 g, 0.0106 mol), and 1,3-thiazole (7.50 mL, 0.106 mol) were dissolved in N,N-dimethylacetamide (40.0 mL). The solution was distributed in equal portions into four 20 mL microwavable vessels. Into each reaction vessel was then added potassium acetate (0.777 g, 7.93 mmol) followed by tetrakis(triphenylphosphine)palladium(0) (0.60 g, 2.1 mmol). Each reaction vessel was heated at 200° C. in the microwave reactor for 30 minutes. The reactions were combined and most of the solvent was removed in vacuo. The residue was diluted with DCM, filtered and concentrated. Purification by flash column chromatography (ethyl acetate/hexanes) afforded the desired product (2.25 g, 64%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08933086B2
Source datasetuspto-grants-2015_01
ORD IDord-59d7d30e3cd54bb2b131e589d2f0810d
Source noteuspto-grants-2015_01