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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1641248Generated: November 2, 2026

N,N,2,2-Tetramethylpropane-1,3-diamine → 4'-Fluoro-2'-methyl-biphenyl-3-carboxylic acid{4-[2-(3-dimethylamino-2,2-dimethyl-propylamino)-pyrimidin-4-yloxy]-naphthalen-1-yl}-amide

https://huagongshe.com/reaction/1641248

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN,N,2,2-Tetramethylpropane-1,3-diamineHCID 104477—
Reactant4'-Fluoro-2'-methyl-biphenyl-3-carboxylic acid [4-(2-methylsulfanylpyrimidin-4-yloxy)-naphthalen-1-yl]-amideHCID 59553187—
Product4'-Fluoro-2'-methyl-biphenyl-3-carboxylic acid{4-[2-(3-dimethylamino-2,2-dimethyl-propylamino)-pyrimidin-4-yloxy]-naphthalen-1-yl}-amideHCID 59553153—

Reaction Steps

Compound is prepared from 4′-fluoro-2′-methyl-biphenyl-3-carboxylic acid[4-(2-methylsulfanyl-pyrimidin-4-yloxy)-naphthalen-1-yl]-amide and N,N,2,2-tetramethyl-1,3-propanediamine according to conditions described in general procedure J. (23 mg). 1H NMR (400 MHz, CDCl3) δ 8.01-8.1(m, 4H), 7.88(dd, 1H, J=0.8 and 8 Hz), 7.5-7.65(m, 5H), 7.26-7.33(m, 2H), 6.98-7.08(m, 2H), 6.21(d, 1H, J=6 Hz), 2.3(s, 3H), 2.0-2.2(brm, 10H), 0.6-0.9(brs, 6H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08114873B2
Source datasetuspto-grants-2012_02
ORD IDord-9fdbeea252f54245ab380934eba61d6d
Source noteuspto-grants-2012_02