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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2237856Generated: October 31, 2026

N-Iodosuccinimide → 5-(4-Chloro-phenyl)-7-cyclopropyl-3-iodo-pyrazolo[1,5-a]pyrimidine

https://huagongshe.com/reaction/2237856

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-IodosuccinimideHCID 120273—
Reactant5-(4-Chloro-phenyl)-7-cyclopropyl-pyrazolo[1,5-a]pyrimidineHCID 67000939—
SolventDimethylformamideHCID 6228—
Product5-(4-Chloro-phenyl)-7-cyclopropyl-3-iodo-pyrazolo[1,5-a]pyrimidineHCID 6700087592%

Reaction Conditions

Temperature20 °C

Reaction Steps

A mixture of 5-(4-chloro-phenyl)-7-cyclopropyl-pyrazolo[1,5-a]pyrimidine (1.08 g, 4.0 mmol) and N-iodo-succinimide (0.90 g, 4.0 mmol) in N,N-dimethylformamide (8 mL) was stirred at 20° C. for 40 min. The heterogeneous mixture was partitioned between EtOAc and water. The organic layer was dried (Na2SO4) and evaporated in vacuo. The residue was triturated with diethyl ether to give 5-(4-chloro-phenyl)-7-cyclopropyl-3-iodo-pyrazolo[1,5-a]pyrimidine (1.45 g, 92%) as a yellow solid. MS (ISP) 395.8 [(M+H)+]; mp 189-190° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07718661B2
Source datasetuspto-grants-2010_05
ORD IDord-8fd53a5cf4434306b0b113070e236bfa
Source noteuspto-grants-2010_05