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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1418005Generated: October 30, 2026

Methylamine → 4-[3'-(3-Methylamino-2-hydroxypropoxy)anilino]6-(3'-methylanilino) pyrimidine

https://huagongshe.com/reaction/1418005

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethylamineHCID 6329—
Reactant4-[3'-(2,3-Epoxypropoxy)anilino]6-(3'-methylanilino) pyrimidineHCID 86753855—
SolventEthanolHCID 702—
SolventWaterHCID 962—
Product4-[3'-(3-Methylamino-2-hydroxypropoxy)anilino]6-(3'-methylanilino) pyrimidineHCID 7018701446%

Reaction Steps

Using an analogous reaction procedure to that described in Example 33, a mixture of 4-[3'-(2,3-epoxypropoxy)anilino]6-(3'-methylanilino) pyrimidine and 33% methylamine in ethanol and NHP was stirred over 2 days at room temperature. The reaction mixture was diluted with water and extracted with ethyl acetate. The product so obtained was washed with water and with brine, dried (MgSO4) and evaporated. The residue was recrystallised from a mixture of methylene chloride, methanol and hexane to give 4-[3'-(3-methylamino-2-hydroxypropoxy)anilino]6-(3'-methylanilino) pyrimidine is 46% yield, m.p. 88°-90° C.;

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05880130
Source datasetuspto-grants-1999_03
ORD IDord-7907808590f3499f9926e9f19ec97b8c
Source noteuspto-grants-1999_03