Guanidine → 4-(2,4-Dimethyl-Thiazol-5-Yl)-Pyrimidin-2-Ylamine
Reaction equation
[CH3:1][C:2]1[N:6]=[C:5]([CH3:7])[S:4][C:3]=1/[CH:8]=[CH:9]/[C:10](N(C)C)=O.[NH2:15][C:16]([NH2:18])=[NH:17]>>[CH3:7][C:5]1[S:4][C:3]([C:8]2[CH:9]=[CH:10][N:15]=[C:16]([NH2:18])[N:17]=2)=[C:2]([CH3:1])[N:6]=1Participants
3
Procedure
This compound was prepared by heating equimolar amounts of 3-dimethylamino-1-(2,4-dimethyl-thiazol-5-yl)-propenone and guanidine in refluxing 2-methoxethanol. 1H-NMR (300 MHz, CDCl3) δ2.67 (s, 3H, CH3), 2.68 (s, 3H, CH3), 5.14 (br, 2H, NH2), 6.83 (d, 1H, J=5.3 Hz, pyrimidinyl-H), 8.30 (d, 1H, J=5.3 Hz, pyrimidinyl-H).
Workup
- customThis compound was prepared
- temperaturein refluxing 2-methoxethanol
Sources & evidence
- ORD record
- ord-8c657b8e0a70442da4fd35d32f80cf70
- Source dataset
- uspto-grants-2004_03
- Patent number
- US06699854B2
Reaction notes
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