3,3-Diphenylpropyl iodide → HCID 70116796, compound
Reaction equation
C([O:3][C:4](=[O:20])[CH2:5][O:6][C:7]1[CH:19]=[CH:18][C:17]2[C:12]3[N:13]=[C:14]([SH:16])[S:15][C:11]=3[CH2:10][C:9]=2[CH:8]=1)C.[C:21]1([CH:27]([C:31]2[CH:36]=[CH:35][CH:34]=[CH:33][CH:32]=2)[CH2:28][CH2:29]I)[CH:26]=[CH:25][CH:24]=[CH:23][CH:22]=1>>[C:21]1([CH:27]([C:31]2[CH:32]=[CH:33][CH:34]=[CH:35][CH:36]=2)[CH2:28][CH2:29][S:16][C:14]2[S:15][C:11]3[CH2:10][C:9]4[CH:8]=[C:7]([O:6][CH2:5][C:4]([OH:3])=[O:20])[CH:19]=[CH:18][C:17]=4[C:12]=3[N:13]=2)[CH:26]=[CH:25][CH:24]=[CH:23][CH:22]=1Participants
3
Procedure
Using ethyl[(2-mercapto-8H-indeno[1,2-d]thiazol-6-yl)oxy]acetate and 3,3-diphenylpropyl iodide, the procedure of Example 21 was otherwise repeated to synthesize-the title compound. Yield 42%.
Sources & evidence
- ORD record
- ord-fadc567f967343f59296b994ff1f8162
- Source dataset
- uspto-grants-2001_06
- Patent number
- US06248766B1
Reaction notes
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