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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 336164Generated: October 30, 2026

Ammonia methanol → 5-iodo-7-((2-(trimethylsilyl)ethoxy)methyl)-7H-pyrrolo[2,3-d]pyrimidin-4-amine

https://huagongshe.com/reaction/336164

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonia methanolHCID 21705897—
Reactant4-chloro-5-iodo-7-((2-(trimethylsilyl)ethoxy)methyl)-7H-pyrrolo[2,3-d]pyrimidineHCID 86706933—
SolventMethanolHCID 887—
SolventWaterHCID 962—
Product5-iodo-7-((2-(trimethylsilyl)ethoxy)methyl)-7H-pyrrolo[2,3-d]pyrimidin-4-amineHCID 68572997—

Reaction Conditions

Temperature120 °C

Reaction Steps

An 8 N ammonia methanol solution (120 ml) was added to the 4-chloro-5-iodo-7-((2-(trimethylsilyl)ethoxy)methyl)-7H-pyrrolo[2,3-d]pyrimidine (20.0 g) obtained in Step 1, and the mixture was stirred in a microwave reactor at 120° C. for 1 hour. After being cooled, the reaction mixture was diluted with methanol (65 ml) and water (185 ml). The resulting precipitate was collected by filtration, washed with water, and dried under reduced pressure to obtain the title compound (15.2 g) as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08889666B2
Source datasetuspto-grants-2014_11
ORD IDord-a80e89840ffd4f02abce38cd30bb1b8d
Source noteuspto-grants-2014_11