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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1272017Generated: October 29, 2026

6-bromo-8-cyclopentyl-5-methyl-2-(methylsulfinyl)pyrido[2,3-d]pyrimidin-7(8H)-one → HCID 10128454, compound

https://huagongshe.com/reaction/1272017

Reaction equation

Participants

RoleNameHCIDCharge
Reactant6-bromo-8-cyclopentyl-5-methyl-2-(methylsulfinyl)pyrido[2,3-d]pyrimidin-7(8H)-oneHCID 11372127—
ReactantHCID 11469830HCID 11469830—
SolventTolueneHCID 1140—
ProductHCID 10128454HCID 1012845427.3%

Reaction Steps

6-Bromo-8-cyclopentyl-2-methanesulfinyl-5-methyl-8H-pyrido[2,3-d]pyrimidin-7-one (1.0 g, 2.70 mmol) and 5-(2,6-dimethyl-morpholin-4-yl)-pyridin-2-ylamine (0.668 g, 3.73 mmol) were heated to reflux in toluene (10 mL) for 16 hours. The reaction mixture was cooled to room temperature and the precipitate that formed was collected by filtration and washed on the funnel with toluene (3×10 mL) to give 6-bromo-8-cyclopentyl-2-[5-(2,6-dimethyl-morpholin-4-yl)-pyridin-2-ylamino]-5-methyl-8H-pyrido[2,3-d]pyrimidin-7-one as a brown solid (0.358 g, 27.3%). MS (APCI) Calc'd for M+1: 513.2. Found: 513.1. Anal. Calc'd for C24H29BrN6O2: C, 56.14; H, 5.69; N, 16.37. Found; C, 55.90; H, 5.62; N, 16.10.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07208489B2
Source datasetuspto-grants-2007_04
ORD IDord-d8040467524042fbbb34e1c9834df19b
Source noteuspto-grants-2007_04