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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1711050Generated: October 30, 2026

Methyl iodide → 4-Chloro-6-(methylthio)thieno[3,2-d]pyrimidine

https://huagongshe.com/reaction/1711050

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantDimethyl DisulfideHCID 12232—
Reactant4-Chlorothieno[3,2-d]pyrimidineHCID 2735821—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
Product4-Chloro-6-(methylthio)thieno[3,2-d]pyrimidineHCID 5942445182%

Reaction Steps

To a solution of 20 (shown in the scheme 4) (200 mg, 1.18 mmol) in THF (11 mL) was added n-BuLi (566 μL, 1.42 mmol, 2.5M in THF) very slowly at −78° C. and the mixture was stirred for 15 min at the same conditions. A solutions of dimethyl disulfide (160 uL, 1.77 mmol) and MeI (110 μL, 1.77 mmol) in THF (1 mL) was added drop wise. The reaction mixture was stirred for 2 h at −78° C., quenched with saturated aqueous NH4Cl solution, and extracted with DCM. The extract was dried over anhydrous Na2SO4 and concentrated to afford the title compound 280 (210 mg, 82% yield) as a yellowish solid. MS (m/z): 217.0 (M+H) (found).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07790729B2
Source datasetuspto-grants-2010_09
ORD IDord-44e475dd0b8f4918b5f487b35012d7f3
Source noteuspto-grants-2010_09