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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 641657Generated: October 31, 2026

Methanol → HCID 68693634, compound

https://huagongshe.com/reaction/641657

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantSodium BicarbonateHCID 516892—
Reactant[3-(Hydroxymethyl)phenyl]boronic acidHCID 2734662—
Reactant6-Bromo-8-cyclopentyl-4-methyl-2-methylamino-8H-pyrido[2,3-d]pyrimidin-7-oneHCID 59258857—
CatalystHCID 178418397HCID 178418397—
SolventTolueneHCID 1140—
ProductHCID 68693634HCID 6869363484.5%

Reaction Steps

6-Bromo-8-cyclopentyl-4-methyl-2-methylamino-8H-pyrido[2,3-d]pyrimidin-7-one (5.00 g, 14.83 mmol), 3-(hydroxymethyl)phenylboronic acid (3.38 g, 22.24 mmol) and Pd(PPh3)4 (0.685 g, 0.593 mmol) were suspended in Toluene (20 mL), MeOH (10 mL) and sat. NaHCO3 (10 mL) and then heated to 100° C. overnight. The reaction was deemed complete by MS and TLC. The organic layer was injected directly onto a column, eluting with CH2Cl2 then 4% MeOH in CH2Cl2. The fractions containing the desired material, as deemed by MS, were combined and evaporated in vacuo to give a greenish beige solid. This was triturated with MeCN and filtered to give crop one, 4.7 g. A second crop was obtained of 0.25 g. A third crop was obtained of 0.10 g. The three crops were deemed to be of sufficient purity based on NMR's and were combined and washed again with MeCN to give a solid (4.39 g, 81.24%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07696213B2
Source datasetuspto-grants-2010_04
ORD IDord-349b07e6235a404c8524096f15dd2c10
Source noteuspto-grants-2010_04