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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1506110Generated: November 2, 2026

Hydrogen iodide → 4-Iodo-7H-pyrrolo(2,3-d)pyrimidine

https://huagongshe.com/reaction/1506110

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrogen iodideHCID 24841—
Reactant7H-Pyrrolo(2,3-d)pyrimidine, 4-chloro-HCID 5356682—
Product4-Iodo-7H-pyrrolo(2,3-d)pyrimidineHCID 5787080496%

Reaction Conditions

Temperature0 °C

Reaction Steps

Hydroiodic acid (55 wt %, 100 g) was mixed with 4-chloro-7H-pyrrolo[2,3-d]pyrimidine (manufactured by Tokyo Chemical Industry Co., Ltd., 10.6 g, 69.0 mmol) under cooling with ice and stirred at 0° C. for 1 hour and then at room temperature for one day. The precipitated solid was collected by filtration and washed with water. The residue was suspended in water, neutralized with 1 M aqueous sodium hydroxide and filtered. The yellow solid was washed with water and dried under reduced pressure to give the title compound as a yellow solid (16.2 g, yield 96%, including 10% 4-chloro-7H-pyrrolo[2,3-d]pyrimidine as the starting compound).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09216999B2
Source datasetuspto-grants-2015_12
ORD IDord-70731825b7e1454280d0d6755c5e076b
Source noteuspto-grants-2015_12