Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1903283Generated: October 31, 2026

4-Iodobenzaldehyde → 2-Amino-5-(p-iodobenzyl)aminomethylpyrrolo[2,3-d]pyrimidin-4-one

https://huagongshe.com/reaction/1903283

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-IodobenzaldehydeHCID 96657—
ReactantSodium borohydrideHCID 4311764—
ReactantSodium MethoxideHCID 10942334—
Reactant2-Amino-5-aminomethylpyrrolo[2,3-d]pyrimidin-4-oneHCID 20246377—
SolventMethanolHCID 887—
Product2-Amino-5-(p-iodobenzyl)aminomethylpyrrolo[2,3-d]pyrimidin-4-oneHCID 2046857161.6%

Reaction Steps

In 40 ml of dry methanol were suspended 126 mg of 2-amino-5-aminomethylpyrrolo[2,3-d]pyrimidin-4-one (dihydrochloride) and 116 mg of p-iodobenzaldehyde. After addition of 1 N methanolic sodium methoxide, the mixture was stirred at room temperature for 30 min. To this mixture was added 76 mg of sodium borohydride and the reaction was conducted at room temperature for 15 min. The reaction was then terminated by addition of 500 mg silica gel. The solvent was distilled off under reduced pressure and the residue was purified by silica gel chromatography to give 121 mg of the desired compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04435570
Source datasetuspto-grants-1984_03
ORD IDord-c036a8432ed64ce7bb8e831aa6ac3d50
Source noteuspto-grants-1984_03