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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2252709Generated: October 26, 2026

Trimethyltin chloride → 5-(Trimethylstannyl)-4-chloro-7H-pyrrolo[2,3-d]pyrimidine

https://huagongshe.com/reaction/2252709

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrimethyltin chlorideHCID 14016—
ReactantAmmonium ChlorideHCID 25517—
Reactant5-Bromo-4-chloro-7H-pyrrolo[2,3-d]pyrimidineHCID 5380710—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
Product5-(Trimethylstannyl)-4-chloro-7H-pyrrolo[2,3-d]pyrimidineHCID 11461236—

Reaction Conditions

Temperature-78 °C

Reaction Steps

To a solution of the compound from Step A (0.92 g, 4 mmol) in THF (25 mL) was added n-BuLi (2.5 M solution in hexane, 3.48 mL) dropwise at −78° C. After the addition, the reaction mixture was stirred at −78° C. for an additional 30 min. To this solution was added trimethyltin chloride (0.88 g, 4.4 mmol) in THF (8 mL) dropwise for a period of 10 min. The reaction mixture was brought to room temperature slowly and stirred at room temperature overnight. Saturated aqueous ammonium chloride (60 mL) was added and extracted with ethyl acetate (3×70 mL). The combined organic extracts were washed with brine, dried over Na2SO4 and evaporated to dryness. The residue was purified over silica gel to give the title compound as a colorless solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07323453B2
Source datasetuspto-grants-2008_01
ORD IDord-3a54b8808b9645c2a9df29a1b12740b8
Source noteuspto-grants-2008_01