Methylamine → HCID 135670774, compound
Reaction equation
CS[C:3]1[N:4]=[N:5][C:6]2[C:12](=[O:13])[NH:11][C:10]([C:14]3[CH:19]=[CH:18][CH:17]=[CH:16][C:15]=3[O:20][CH2:21][CH2:22][CH3:23])=[N:9][C:7]=2[N:8]=1.[CH3:24][NH2:25]>C(Cl)(Cl)Cl>[CH3:24][NH:25][C:3]1[N:4]=[N:5][C:6]2[C:12](=[O:13])[NH:11][C:10]([C:14]3[CH:19]=[CH:18][CH:17]=[CH:16][C:15]=3[O:20][CH2:21][CH2:22][CH3:23])=[N:9][C:7]=2[N:8]=1Participants
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
3-Methylthio-8-oxo-6-(2-propoxyphenyl)-7,8-dihydropyrimido[4,5-e][1,2,4]triazine (2.0 g) was treated with a solution of methylamine in industrial methylated spirit (33%, 30 ml) at 75° C. in a pressure vessel for 20 hours. The cooled reaction mixture was evaporated under reduced pressure to afford an oily solid which was dissolved in chloroform. The organic solution was washed with water, dried and evaporated under reduced pressure to afford a yellow oily solid which was eluted from a silica column with chloroform/methanol (5%). The fractions containing product were combined and evaporated under reduced pressure to afford a yellow solid (180 mg) which together with another sample (50 mg), similarly prepared, was recrystallized from ethanol to afford the title compound, 140 mg, m.p. 261-263° C.
Workup
- customThe cooled reaction mixture
- customwas evaporated under reduced pressure
- customto afford an oily solid which
- washThe organic solution was washed with water
- customdried
- customevaporated under reduced pressure
- customto afford a yellow oily solid which
- washwas eluted from a silica column with chloroform/methanol (5%)
- additionThe fractions containing product
- customevaporated under reduced pressure
Sources & evidence
- ORD record
- ord-0ab53ea499cb4ce2ad93a72fcce5467b
- Source dataset
- uspto-grants-2002_05
- Patent number
- US06391885B1
Reaction notes
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