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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1487243Generated: October 30, 2026

N-Iodosuccinimide → 2-Butyl-4-chloro-7-iodo-5H-pyrrolo[3,2-d]pyrimidine

https://huagongshe.com/reaction/1487243

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-IodosuccinimideHCID 120273—
Reactant2-Butyl-4-chloro-5H-pyrrolo[3,2-d]pyrimidineHCID 118382848—
SolventTetrahydrofuranHCID 8028—
Solventtert-Butyl methyl etherHCID 15413—
Product2-Butyl-4-chloro-7-iodo-5H-pyrrolo[3,2-d]pyrimidineHCID 11838284781.3%

Reaction Steps

N-Iodosuccinimide (2.09 g, 9.29 mmol) was added portionwise to a stirred solution of 2-butyl-4-chloro-5H-pyrrolo[3,2-d]pyrimidine (1.69 g, 8.06 mmol) in THF (35 mL). The resultant mixture was stirred at room temperature for 1 hour. The reaction mixture was diluted with TBME (50 mL) then washed with aqueous sodium thiosulphate solution (50 mL) then saturated aqueous sodium chloride solution (20 mL). The organic phase was dried (Na2SO4), filtered and evaporated. The sample was dissolved in dichloromethane and purified by chromatography on silica using a gradient of 0-100% dichloromethane-cyclohexane over 30 minutes followed by a gradient of 0-100% TBME-cyclohexane followed by 0-20% methanol over 15 minutes. The appropriate fractions were identified by LC-MS then combined and evaporated in vacuo to give the title compound as a yellow solid (2.2 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09428512B2
Source datasetuspto-grants-2016_08
ORD IDord-42c0e598aeba4a2cae89c79fd0efaa12
Source noteuspto-grants-2016_08