6-(2,4-difluorophenoxy)-8-methyl-2-(piperidin-4-ylamino)-8H-pyrido[2,3-d]pyrimidin-7-one

Base Information

• Chemical Name: 6-(2,4-difluorophenoxy)-8-methyl-2-(piperidin-4-ylamino)-8H-pyrido[2,3-d]pyrimidin-7-one
• CAS No.: 1280218-56-5
• Molecular Formula: C₁₉H₁₉F₂N₅O₂
• Molecular Weight: 387.389
• Mol file: 1280218-56-5.mol

Synonyms:6-(2,4-difluorophenoxy)-8-methyl-2-(piperidin-4-ylamino)-8H-pyrido[2,3-d]pyrimidin-7-one

Chemical Property of 6-(2,4-difluorophenoxy)-8-methyl-2-(piperidin-4-ylamino)-8H-pyrido[2,3-d]pyrimidin-7-one

Chemical Property:

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

Technology Process of 6-(2,4-difluorophenoxy)-8-methyl-2-(piperidin-4-ylamino)-8H-pyrido[2,3-d]pyrimidin-7-one

There total 9 articles about 6-(2,4-difluorophenoxy)-8-methyl-2-(piperidin-4-ylamino)-8H-pyrido[2,3-d]pyrimidin-7-one which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield:

4-aminopiperidine (13035-19-3) + 6-(2,4-difluorophenoxy)-8-methyl-2-(methylsulfonyl)pyrido[2,3-d]pyrimidin-7(8H)-one (449808-50-8) → 6-(2,4-difluorophenoxy)-8-methyl-2-(piperidin-4-ylamino)-8H-pyrido[2,3-d]pyrimidin-7-one (1280218-56-5)

Guidance literature:

With N-ethyl-N,N-diisopropylamine; In isopropyl alcohol; for 36h; Reflux;

DOI:10.1016/j.bmcl.2015.11.099

Reference yield:

4-methylamino-2-methylthiopyrimidine-5-carboxaldehyde (185040-32-8) → 6-(2,4-difluorophenoxy)-8-methyl-2-(piperidin-4-ylamino)-8H-pyrido[2,3-d]pyrimidin-7-one (1280218-56-5)

Guidance literature:

Multi-step reaction with 4 steps

1: potassium carbonate / 1-methyl-pyrrolidin-2-one / 18 h / 120 °C

2: formic acid; dihydrogen peroxide / dichloromethane; water / 38 °C

3: sodium carbonate / tetrahydrofuran; methanol / 120 h / 20 °C

4: 2-Chloroethyl chloroformate / 1,2-dichloro-ethane / 48 h / Reflux

With formic acid; dihydrogen peroxide; sodium carbonate; potassium carbonate; 2-Chloroethyl chloroformate; In tetrahydrofuran; 1-methyl-pyrrolidin-2-one; methanol; dichloromethane; water; 1,2-dichloro-ethane;

DOI:10.1021/jm101423y

Reference yield:

6?(2,4?difluorophenoxy)?8?methyl?2?(methylthio)pyrido[2,3?d]pyrimidin?7(8H)?one (449811-12-5) → 6-(2,4-difluorophenoxy)-8-methyl-2-(piperidin-4-ylamino)-8H-pyrido[2,3-d]pyrimidin-7-one (1280218-56-5)

Guidance literature:

Multi-step reaction with 3 steps

1: formic acid; dihydrogen peroxide / dichloromethane; water / 38 °C

2: sodium carbonate / tetrahydrofuran; methanol / 120 h / 20 °C

3: 2-Chloroethyl chloroformate / 1,2-dichloro-ethane / 48 h / Reflux

With formic acid; dihydrogen peroxide; sodium carbonate; 2-Chloroethyl chloroformate; In tetrahydrofuran; methanol; dichloromethane; water; 1,2-dichloro-ethane;

DOI:10.1021/jm101423y

upstream raw materials:

6-(2,4-difluorophenoxy)-8-methyl-2-(methylsulfonyl)pyrido[2,3-d]pyrimidin-7(8H)-one

2-(1-benzylpiperidin-4-ylamino)-6-(2,4-difluorophenoxy)-8-methyl-8H-pyrido[2,3-d]pyrimidin-7-one

6?(2,4?difluorophenoxy)?8?methyl?2?(methylthio)pyrido[2,3?d]pyrimidin?7(8H)?one

(4-methylamino-2-methylsulfanyl-pyrimidin-5-yl)-methanol

Downstream raw materials:

2-(1-acetylpiperidin-4-ylamino)-6-(2,4-difluorophenoxy)-8-methyl-8H-pyrido[2,3-d]pyrimidin-7-one