Thiophenol → HCID 18507469, compound
Reaction equation
[Br:1][C:2]1[C:3]([C:12]2[O:13][CH:14]=[CH:15][CH:16]=2)=[N:4][C:5]([NH2:11])=[N:6][C:7]=1[S:8]([CH3:10])=O.[C:17]1(S)[CH:22]=[CH:21]C=[CH:19][CH:18]=1.C1CCN2C(=NCCC2)CC1>O1CCOCC1>[Br:1][C:2]1[C:3]([C:12]2[O:13][CH:14]=[CH:15][CH:16]=2)=[N:4][C:5]([NH2:11])=[N:6][C:7]=1[S:8][C:10]1[CH:21]=[CH:22][CH:17]=[CH:18][CH:19]=1Participants
5
Reactant 3
Product 1
Reagents, catalysts & solvents 1
Procedure
From 5-bromo-4-furan-2-yl-6-methanesulfinyl-pyrimidin-2-yl-amine, thiophenol and DBU in dioxane. EI-MS m/e (%): 349 (M{81Br}+, 40), 348 ([M{81Br}-H]+, 28), 347 (M{79Br}+, 39), 346 ([M{79Br}-H]+, 24), 268 ([M—Br]+, 100), 175 (92).
Sources & evidence
- ORD record
- ord-a49202af6331445abfcaaf9e860f2f8b
- Source dataset
- uspto-grants-2003_07
- Patent number
- US06586441B2
Reaction notes
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