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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1640703Generated: November 4, 2026

2,4-Dichloropyrimidine → HCID 178434332, compound

https://huagongshe.com/reaction/1640703

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 numberUS08114885B2
Source datasetuspto-grants-2012_02
ORD IDord-1aa047ee8e32422c92e36fd97f0ee409
Source noteuspto-grants-2012_02