(3-Iodophenyl)(isocyano)methyl 4-methylphenyl sulfone → 6-(4-(3-iodophenyl)-1-methyl-1H-imidazol-5-yl)-4-(methylthio)thieno[2,3-d]pyrimidine
Reaction equation
[CH3:1][S:2][C:3]1[C:4]2[CH:11]=[C:10]([CH:12]=[N:13][CH3:14])[S:9][C:5]=2[N:6]=[CH:7][N:8]=1.COC1C=C(C=CC=1OC)CN=CC1SC2N=CN=CC=2C=1.CC1C=CC(S([CH:47]([C:50]2[CH:55]=[CH:54][CH:53]=[C:52]([I:56])[CH:51]=2)[N+:48]#[C-:49])(=O)=O)=CC=1>>[I:56][C:52]1[CH:51]=[C:50]([C:47]2[N:48]=[CH:49][N:13]([CH3:14])[C:12]=2[C:10]2[S:9][C:5]3[N:6]=[CH:7][N:8]=[C:3]([S:2][CH3:1])[C:4]=3[CH:11]=2)[CH:55]=[CH:54][CH:53]=1Participants
4
Reactant 3
Product 1
Procedure
The title compound was prepared by a similar process to that described for Example 6 but using N-[4-(methylthio)thieno[2,3-d]pyrimidin-6-ylmethylidene]methanamine (Intermediate 16) in place of N-(3,4-Dimethoxybenzyl)-N-[thieno[2,3-d]pyrimidin-6-ylmethylidene]amine (intermediate 14) and using (3-iodophenyl)(isocyano)methyl 4-methylphenyl sulfone (Intermediate 53) in place of PhTosMIC. Pale yellow solid (1.50 g, 71%);
Sources & evidence
- ORD record
- ord-fff338ca9eaf45a79cf4bfcd9da92dee
- Source dataset
- uspto-grants-2008_09
- Patent number
- US07427616B2
Reaction notes
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