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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 586484Generated: October 27, 2026

2-Aminopyridine → 6-Bromo-8-cyclopentyl-2-(pyridin-2-ylamino)-8H-pyrido[2,3-d]pyrimidin-7-one

https://huagongshe.com/reaction/586484

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-AminopyridineHCID 10439—
Reactant6-bromo-8-cyclopentyl-2-methanesulfinyl-8H-pyrido[2,3-d]pyrimidin-7-oneHCID 11428232—
Product6-Bromo-8-cyclopentyl-2-(pyridin-2-ylamino)-8H-pyrido[2,3-d]pyrimidin-7-oneHCID 533028237%

Reaction Steps

6-Bromo-8-cyclopentyl-2-methanesulfinyl-8H-pyrido[2,3-d]pyrimidin-7-one and 2-aminopyridine were reacted according to the procedure outlined in Example 37 to provide 6-bromo-8-cyclopentyl-2-(pyridin-2-ylamino)-8H-pyrido[2,3-d]pyrimidin-7-one in 37% yield. mp: 273˜275° C. Anal. Calc'd for C17H16BrN5O.0.1H2O: C, 52.62; H, 4.21; N, 18.05. Found: C, 52.23; H, 4.10; N, 17.91. M++1: Calc'd: 386.05, Found 385.9.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06936612B2
Source datasetuspto-grants-2005_08
ORD IDord-a1d1d2fde231415a8af90cf6eca6b278
Source noteuspto-grants-2005_08