Thenyl mercaptan → 4-[[(1R)-2-Hydroxy-1-methylethyl]amino]-2-[[(2-thienyl)methyl)thio]-7(8H)-pteridinone
Reaction equation
F[C:2]1[C:7](F)=[CH:6]C=C[C:3]=1[CH2:9][S:10]([C:13]1[N:22]=[C:21]([NH:23][C@H:24]([CH3:27])[CH2:25][OH:26])[C:20]2[N:19]=[CH:18][C:17](=[O:28])[NH:16][C:15]=2[N:14]=1)(=O)=O.[S:29]1C=CC=C1CS>>[OH:26][CH2:25][C@H:24]([NH:23][C:21]1[C:20]2[N:19]=[CH:18][C:17](=[O:28])[NH:16][C:15]=2[N:14]=[C:13]([S:10][CH2:9][C:3]2[S:29][CH:6]=[CH:7][CH:2]=2)[N:22]=1)[CH3:27]Participants
3
Procedure
The titled compound (0.076 g) was prepared by the method of Example 13, step (c) using the product from Example 13, step (a) (0.20 g) and 2-thienylmethylmercaptan (0.050 g).
Sources & evidence
- ORD record
- ord-7351a331112e499eb71703af752f1a2c
- Source dataset
- uspto-grants-2009_08
- Patent number
- US07579342B2
Reaction notes
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