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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 855624Generated: November 1, 2026

2,4-Dichloropyrimidine → HCID 178434332, compound

https://huagongshe.com/reaction/855624

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,4-DichloropyrimidineHCID 77531—
ReactantSodium BicarbonateHCID 516892—
ReactantHCID 178434350HCID 178434350—
SolventEthanolHCID 702—
SolventTetrahydrofuranHCID 8028—
ProductHCID 178434332HCID 17843433289.8%

Reaction Steps

To a stirred solution of 3-methyl-6-aminoindazole (2.71 g, 0.015 mol) and NaHCO3 (1.26 g, 0.045 mol) in THF (15 mL) and ethanol (60 mL) was added 2,4-dichloropyrimidine (6.66 g, 0.045 mol) at room temperature. After the reaction was stirred for four hours, the suspension was filtered and washed thoroughly with ethanol. The filtrate was concentrated under reduced pressure, and the resulting solid was washed with ether to remove excess pyrimidine to yield 3.5 g (89% yield) of N-(2-chloro-4-pyrimidinyl)-N-(3-methyl-1H-indazol-6-yl)amine.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07262203B2
Source datasetuspto-grants-2007_08
ORD IDord-29bd22c63143425d9ff5236b3bcbe392
Source noteuspto-grants-2007_08