Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1913922Generated: November 2, 2026

Tetrahydrofuran → 2-Cyclohexyl-5-[(2-methyl-1,3-thiazol-4-yl)ethynyl]pyrimidine

https://huagongshe.com/reaction/1913922

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
Reactant2-Chloro-5-[(2-methyl-1,3-thiazol-4-yl)ethynyl]pyrimidineHCID 57823029—
ReactantHCID 178418970HCID 178418970—
CatalystHCID 178418397HCID 178418397—
Product2-Cyclohexyl-5-[(2-methyl-1,3-thiazol-4-yl)ethynyl]pyrimidineHCID 16663138—

Reaction Conditions

Temperature150 °C

Reaction Steps

200 mg (0.85 mmol, 1 eq) 2-chloro-5-[(2-methyl-1,3-thiazol-4-yl)ethynyl]pyrimidine, 50 mg (0.043 mmol, 0.05 eq) tetrakis(triphenylphosphine)palladium(0), and 2 mL of 0.5 M cyclohexylzinc bromide in THF (1 mmol, 1.1 eq) were combined. The reaction mixture was heated at 150° C. in the microwave for 5 min, quenched with pH 10 PBS, extracted with DCM. Silica gel chromatography (gradient 10% to 40% EtOAc/Hexanes) gave 2-cyclohexyl-5-[(2-methyl-1,3-thiazol-4-yl)ethynyl]pyrimidine (L-001152744). LC-MS calculated for C16H17N3S 283, observed m/e 284.1 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08609852B2
Source datasetuspto-grants-2013_12
ORD IDord-72a9fdf0bbd44b638138b57bcc3c0a53
Source noteuspto-grants-2013_12