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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1685177Generated: October 26, 2026

Methyl iodide → 4-Chloro-5-methyl-5H-pyrrolo[2,3-d]pyrimidin-6(7H)-one

https://huagongshe.com/reaction/1685177

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantLithium HexamethyldisilazideHCID 2733832—
Reactant4-chloro-5H,6H,7H-pyrrolo[2,3-d]pyrimidin-6-oneHCID 12095870—
SolventTetrahydrofuranHCID 8028—
Product4-Chloro-5-methyl-5H-pyrrolo[2,3-d]pyrimidin-6(7H)-oneHCID 5932245356.8%

Reaction Conditions

Temperature-78 °C

Reaction Steps

Add 4-chloro-5,7-dihydro-pyrrolo[2,3-d]pyrimidin-6-one (0.4 g; 0.0023 mol; 1.0 equiv) in THF (15 mL) and cool to −78° C. under an argon atmosphere. Add drop-wise lithium hexamethyldisilazide (4.7 mL; 0.0047 mol; 2.0 equiv; 1 M in THF). Stir the reaction at −78° C. for 30 min. Add drop-wise methyl iodide (0.29 mL; 0.0047 mol; 2.0 equiv), allow the reaction temperature to come to −20° C. slowly and stir at −20° C. for 2 h. Quench the reaction with saturated ammonium chloride aqueous and extract with EA. Evaporate the organic layer to give the title compound (0.24 g; 41.38%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08148387B2
Source datasetuspto-grants-2012_04
ORD IDord-e90c8c31da5343f0a55e99de79c22cdc
Source noteuspto-grants-2012_04