2-chloro-8-cyclopentyl-5-Methylpyrido[2,3-d]pyriMidin-7(8H)-one synthesis
- Product Name:2-chloro-8-cyclopentyl-5-Methylpyrido[2,3-d]pyriMidin-7(8H)-one
- CAS Number:1013916-37-4
- Molecular formula:C13H14ClN3O
- Molecular Weight:263.72
733039-20-8
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107-93-7
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1013916-37-4
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Yield:1013916-37-4 81%
Reaction Conditions:
Stage #1:5-bromo-2-chloro-N-cyclopentylaminopyrimidine-4-amine;(E)-but-2-enoic acid with palladium diacetate;triethylamine in 1-methyl-pyrrolidin-2-one at 65;Inert atmosphere;
Stage #2: with acetic anhydride in 1-methyl-pyrrolidin-2-one at 65;Inert atmosphere;
Steps:
2.B Preparation of 2-chloro-8-cvclopentyl-5-methyl-8H-pyrido[2,3-d]pyrimidin-7-one
To a vessel was added 5-bromo-2-chloro-6-cyclopentylamino-pyridimidine (10.0 g, 1.0 equiv.) along with N-methylpyrrolidone (NMP) (50 mL, 5.0 vol.) at ambient temperature. To the reaction mixture was added crotonic acid (4.7 g, 1.5 equiv.) and triethylamine (20.2 mL, 4.0 equiv.). The vessel was degassed and purged three times with nitrogen. To the degassed reaction mixture was added Pd(OAc)2(0.25 g, 0.03 equiv.). The vessel was degassed and purged three times with nitrogen using the same method as step 3. The mixture was heated to 65°C and allowed to stir until starting material was consumed (at least 6 hours).Acetic anhydride (6.8 mL, 2.0 equiv) was added to the reaction mixture. The reaction was allowed to react at 65 °C until starting material was consumed (usually 1-2 hours). The reaction mixture was cooled to 20°C and H20 (100 mL, 10 vol) was added to dissolve triethylamine-HBr salts and precipitate out 2-chloro-8-cyclopentyl-5-methyl-8/-/- pyrido[2,3-c]pyrimidin-7-one. The material was granulated at 20 °C for 1 hour. The solids were filtered and washed with H20 (20 mL, 2.0 vol), and a 4: 1 mixture of isopropanol/H20 (50 mL, 5.0 vol). The crude product was dried under vacuum at 55-70°C to give 2-chloro-8-cyclopentyl-5- methyl-8/-/-pyrido[2,3-c]pyrimidin-7-one, (7.8 g; 81 %) as a tan to gray solid.
References:
PFIZER INC.;CHEKAL, Brian Patrick;IDE, Nathan D. WO2014/128588, 2014, A1 Location in patent:Page/Page column 34; 35
3724-65-0
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733039-20-8
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1013916-37-4
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$25.00/5g
1003-03-8
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1013916-37-4
263 suppliers
$25.00/5g
733039-20-8
265 suppliers
$6.00/1g
1013916-37-4
263 suppliers
$25.00/5g