Methylamine → Ethyl 4-(methylamino)-2-(methylsulfanyl)pyrimidine-5-carboxylate
Reaction equation
[CH2:1]([O:3][C:4]([C:6]1[C:7](Cl)=[N:8][C:9]([S:12][CH3:13])=[N:10][CH:11]=1)=[O:5])[CH3:2].CN.[CH2:17]([N:19](CC)CC)C>O1CCCC1>[CH2:1]([O:3][C:4]([C:6]1[C:7]([NH:19][CH3:17])=[N:8][C:9]([S:12][CH3:13])=[N:10][CH:11]=1)=[O:5])[CH3:2]Participants
5
Procedure
4-Methylamino-2-methylsulfanylpyrimidine-5-carboxylic acid ethyl ester was prepared from 4-chloro-2-methylsulfanyl-pyrimidine-5-carboxylic acid ethyl ester and methylamine in tetrahydrofuran (THF) under basic conditions with triethylamine at temperatures between 5° C. and room temperature (RT).
Sources & evidence
- ORD record
- ord-0e04331229534587be49008e2fe85225
- Source dataset
- uspto-grants-2010_02
- Patent number
- US07655651B2
Reaction notes
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