Benzylamine → 2-Amino-4-benzylamino-6-(3-methyl-furan-2-yl)-pyrimidine-5-carbonitrile
Reaction equation
[NH2:1][C:2]1[N:7]=[C:6]([C:8]2[O:9][CH:10]=[CH:11][C:12]=2[CH3:13])[C:5]([C:14]#[N:15])=[C:4](SC)[N:3]=1.[CH2:18]([NH2:25])[C:19]1[CH:24]=[CH:23][CH:22]=[CH:21][CH:20]=1>COCCOC>[NH2:1][C:2]1[N:3]=[C:4]([NH:25][CH2:18][C:19]2[CH:24]=[CH:23][CH:22]=[CH:21][CH:20]=2)[C:5]([C:14]#[N:15])=[C:6]([C:8]2[O:9][CH:10]=[CH:11][C:12]=2[CH3:13])[N:7]=1Participants
4
Procedure
From 2-amino-4-(3-methyl-furan-2-yl)-6-methylsulfanyl-pyrimidine-5-carbonitrile and benzylamine in DME. EI-MS m/e (%): 305 (M+, 40), 304 ([M—H]+, 100).
Sources & evidence
- ORD record
- ord-9e038cffb268487ea89155d9b33fbb6b
- Source dataset
- uspto-grants-2003_07
- Patent number
- US06586441B2
Reaction notes
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