Reaction equation
[CH2:1]([C:5]1[N:6]([CH2:23][C:24]2[CH:29]=[CH:28][CH:27]=[CH:26][C:25]=2[Cl:30])[C:7](/[CH:10]=[C:11](\[CH2:17][C:18]2[S:19][CH:20]=[CH:21][CH:22]=2)/[CH:12]([CH3:16])[C:13]([OH:15])=[O:14])=[CH:8][N:9]=1)[CH2:2][CH2:3][CH3:4].ClC[C:33]1[S:34][CH:35]=[CH:36][CH:37]=1>>[CH2:1]([C:5]1[N:6]([CH2:23][C:24]2[CH:29]=[CH:28][CH:27]=[CH:26][C:25]=2[Cl:30])[C:7](/[CH:10]=[C:11](\[CH2:17][C:18]2[S:19][CH:20]=[CH:21][CH:22]=2)/[CH:12]([CH2:16][C:33]2[S:34][CH:35]=[CH:36][CH:37]=2)[C:13]([OH:15])=[O:14])=[CH:8][N:9]=1)[CH2:2][CH2:3][CH3:4]Participants
3
Reactant 2
Product 1
Procedure
This compound is prepared according to the procedure of Example 14(i, ii) using less than one equivalent of 2-chloromethylthiophene in place of methyl iodide.
Workup
- customThis compound is prepared
Sources & evidence
- ORD record
- ord-07ee8a774b9b4c79a8437c6eba64e690
- Source dataset
- uspto-grants-1995_05
- Patent number
- US05418250
Linked notes
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