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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1655570Generated: November 2, 2026

Methylamine → HCID 19791721, compound

https://huagongshe.com/reaction/1655570

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethylamineHCID 6329—
ReactantTetrahydrofuranHCID 8028—
ReactantHCID 19791826HCID 19791826—
ProductHCID 19791721HCID 19791721—

Reaction Steps

4-Bromomethyl-2-nitrobiphenyl, prpepared as described by D. J. Carini, et al. D. J. Carini, et al. on page 105 in European Application Number 324,377 published Jul. 19, 1989, is reacted with excess methylamine in THF in a manner similar to that described in Example 18A, to give 4'-methylaminomethyl-2-nitrobiphenyl. 4'-Methylaminomethyl-2-nitrobiphenyl is reacted, according to the procedures described in Example 1C, with ethyl 2-butyl-4-chloropyrimidine-5-carboxylate to give ethyl 2-butyl-4-{N-[N-methyl-(2'-nitrobiphenyl-4-yl)methyl]amino)pyrimidine-5-carboxylate. Hydrogenation over palladium on carbon in methanol gives the intermediate ethyl 2-butyl-4-{N-[methyl-(2'-aminobiphenyl-4-yl)methyl]amino}pyrimidine-5-carboxylate. The intermediate is dissolved in methylene chloride containing triethylamine and treated at low temperature with trifluoromethanesulfonyl chloride to give the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05250548
Source datasetuspto-grants-1993_10
ORD IDord-2c64c7fa5286475aac62911b81400b68
Source noteuspto-grants-1993_10