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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1051482Generated: October 25, 2026

Methyl iodide → 2-Chloro-7-methyl-7H-pyrrolo(2,3-d)pyrimidine

https://huagongshe.com/reaction/1051482

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantSodium hydrideHCID 24758—
Reactant2-Chloro-7H-pyrrolo[2,3-d]pyrimidineHCID 5706774—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
Product2-Chloro-7-methyl-7H-pyrrolo(2,3-d)pyrimidineHCID 5741588859.7%

Reaction Steps

To a solution of NaH (106.6 mg, 2.67 mmol) in THF (5 mL) was added 2-chloro-7H-pyrrolo[2,3-d]pyrimidine (500 mg, 2.54 mmol) at 0° C. and stirred for 30 minutes at the same temperature. CH3I (1.5 g, 10.2 mmol) was added at 0° C. and the combined mixture stirred for 3 h at 15° C. After TLC showed the reaction was complete, the mixture was diluted with water 20 mL) and extracted with ethyl acetate EA (2×20 mL) and the combined organic layers were washed with brine (30 mL), dried over Na2SO4 and concentrated to give the title compound (254 mg, 47.4%) as colorless oil which was used in next step without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09388173B2
Source datasetuspto-grants-2016_07
ORD IDord-d4f396a6a4cd462b933d766abc1c53cb
Source noteuspto-grants-2016_07