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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 275967Generated: November 1, 2026

Chloromethyl Methyl Ether → HCID 18315823, compound

https://huagongshe.com/reaction/275967

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChloromethyl Methyl EtherHCID 7864—
ReactantHCID 18315741HCID 18315741—
SolventDiethyl EtherHCID 3283—
ProductHCID 18315823HCID 183158230.05%

Reaction Conditions

Temperature80 °C

Reaction Steps

2-(4-Fluorophenylamino)-6-methyl-4-(1-methyl-1,2,3,4-tetrahydroisoquino-line-2-yl)pyrimidine (0.9 g, 2.58 mmol) was added to chloromethyl methyl ether (3 ml) in a sealed tube. The mixture was stirred at 80° C. for 1 day. After cooling to room temperature, ethyl ether was added to mixture. Resulting solid was removed by filtration. Filtrate was washed with aqueous 2N NaOH solution, dried over sodium sulfate, and concentrated under reduced pressure. Crude product was purified with a silica gel column chromatography (eluent: ethyl acttate:hexane=1:3). Purified compound was treated with HCl solution in ethyl ether. Precipitated solid was isolated by filtration, washed with ethyl ether, and dried in vacuum. It gave 0.6 mg of the titled compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06352993B1
Source datasetuspto-grants-2002_03
ORD IDord-976615a521d04ca3a1ffe6d6eaf00cca
Source noteuspto-grants-2002_03