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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 30083Generated: October 26, 2026

Diphenyl N-Cyanocarbonimidate → Phenyl N-cyano-N'-(2-{[8-(2,6-difluorophenyl)-4-(4-fluoro-2-methylphenyl)-7-oxo-7,8-dihydropyrido[2,3-d]pyrimidin-2-yl]amino}ethyl)imidocarbamate

https://huagongshe.com/reaction/30083

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiphenyl N-CyanocarbonimidateHCID 688090—
Reactant2-[(2-Aminoethyl)amino]-8-(2,6-difluorophenyl)-4-(4-fluoro-2-methylphenyl)pyrido[2,3-d]pyrimidin-7(8H)-oneHCID 59639577—
SolventIsopropanolHCID 3776—
ProductPhenyl N-cyano-N'-(2-{[8-(2,6-difluorophenyl)-4-(4-fluoro-2-methylphenyl)-7-oxo-7,8-dihydropyrido[2,3-d]pyrimidin-2-yl]amino}ethyl)imidocarbamateHCID 59789334—

Reaction Steps

The title compound from Example 8 [8-(2,6-Difluorophenyl)-4-(4-fluoro-2-methylphenyl)-2-[(2-aminoethyl)amino]-8H-pyrido[2,3-d]pyrimidin-7-one](0.382 g, 0.0009 mol) was treated with stirring with diphenylcyanocarbonimidate (0.214 g, 0.0009 mol) in isopropanol (5 mL). Stirred at 23° for 0.5 hours. LC/MS showed a new major peak corresponding to the desired product and no starting material in the solution. LC MS (m/e)=570(MH+). Rt=2.24 min.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07423042B2
Source datasetuspto-grants-2008_09
ORD IDord-a6eb4884d534449dbc2caff6019af854
Source noteuspto-grants-2008_09