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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 29818Generated: October 26, 2026

Methylamine → 2-chloro-N-methyl-5-nitropyrimidin-4-amine

https://huagongshe.com/reaction/29818

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethylamineHCID 6329—
Reactant2,4-Dichloro-5-nitropyrimidineHCID 521266—
SolventTetrahydrofuranHCID 8028—
Product2-chloro-N-methyl-5-nitropyrimidin-4-amineHCID 714723299.3%

Reaction Steps

A solution of 2,4-dichloro-5-nitropyrimidine (7.26 g, 37.4 mmol) in THF (100 ml) is cooled to −78° C. A solution of methyl amine (8 M in methanol, 9.35 mL, 74.8 mmol) is added dropwise. The mixture is allowed to warm to room temperature, and concentrated. The residue is partitioned between ethyl acetate and water. The layer is separated and the aqueous layer is extracted with ethyl acetate. The combined organic extracts are washed with brine, dried over Na2SO4, filtered and concentrated to afford the title product (7.0 g). (Note: the product contains 5% regio-isomer, 4-chloro-2-(methylamino)-5-nitropyrimidine). The residue is used in the next step without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07423038B2
Source datasetuspto-grants-2008_09
ORD IDord-83d91350d3d04fa4bc5182a219334930
Source noteuspto-grants-2008_09