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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 131193Generated: October 25, 2026

Thiazole → 2-Chloro-4-(2-thiazolyl)thieno[3,2-d]pyrimidine

https://huagongshe.com/reaction/131193

Reaction equation

Participants

RoleNameHCIDCharge
ReactantThiazoleHCID 9256—
Reactant2,4-Dichlorothieno[3,2-d]pyrimidineHCID 12712832—
ReactantButyllithiumHCID 178418339—
CatalystZincchlorideHCID 3007855—
CatalystHCID 178418397HCID 178418397—
SolventTetrahydrofuranHCID 8028—
SolventAmmonium ChlorideHCID 25517—
Product2-Chloro-4-(2-thiazolyl)thieno[3,2-d]pyrimidineHCID 4444956529.6%

Reaction Steps

A stirred solution of thiazole (0.14 mL, 2 mmol) in dry THF (10 mL) at −78° C., under argon was treated with n-BuLi (1.6-M in hexanes, 1.3 mL, 2 mmol), stirred for 30 min, treated with a solution of ZnCl2 (1.0-M in Et2O, 2.0 mL, 2 mmol) and allowed to warm gradually to room temperature. The mixture was treated with a solution of 2,4-dichlorothieno[3,2-d]pyrimidine (205 mg, 1 mmol) in THF (5 mL) then Pd(PPh3)4 (100 mg, 10 mol %) refluxed for 17 h, cooled, diluted with saturated NH4Cl solution and extracted with EtOAc. The organic extracts were dried (MgSO4), concentrated in vacuo and purified by chromatography [SiO2; isohexane:CH2Cl2 (2:1)] to give the title compound (75 mg, 26%) as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07384949B2
Source datasetuspto-grants-2008_06
ORD IDord-96f2a38021b84d41893b9f04c1daf11c
Source noteuspto-grants-2008_06