Ethylamine → HCID 18374883, compound
Reaction equation
[CH3:1][N:2]1[C:7]2[N:8]=[C:9](S(C)(=O)=O)[N:10]=[CH:11][C:6]=2[CH:5]=[CH:4][C:3]1=[O:16].[CH2:17]([NH2:19])[CH3:18]>>[CH2:17]([NH:19][C:9]1[N:10]=[CH:11][C:6]2[CH:5]=[CH:4][C:3](=[O:16])[N:2]([CH3:1])[C:7]=2[N:8]=1)[CH3:18]Participants
3
Procedure
A mixture of 8-methyl-2-methanesulfonyl-8H-pyrido[2,3-d]pyrimidin-7-one (152 mg, 0.63 mmol) in 2.5 mL of 70% aqueous ethylamine was stirred at room temperature for 10 minutes. The reaction mixture was partitioned between ethyl acetate and water, and the organic layer was washed with saturated sodium bicarbonate and brine, dried over magnesium sulfate, and concentrated in vacuo to give 105 mg (82%) of 2-ethylamino 8-methyl-8H-pyrido[2,3-d]pyrimidin-7-one, mp 194-195° C.
Workup
- customThe reaction mixture was partitioned between ethyl acetate and water
- washthe organic layer was washed with saturated sodium bicarbonate and brine
- dry with materialdried over magnesium sulfate
- concentrationconcentrated in vacuo
Sources & evidence
- ORD record
- ord-b9c667cd1a654c8f91da9df3f7754d75
- Source dataset
- uspto-grants-2002_12
- Patent number
- US06498163B1
Reaction notes
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