1-[2-(3-chloropropyl)-2,3-dihydro-1H-isoindol-5-yl]propan-1-one → 1-(2-{3-[(4-Methyl-5-phenyl-4H-1,2,4-triazol-3-yl)thio]propyl}-2,3-dihydro-1H-isoindol-5-yl)propan-1-one hydrochloride
Reaction equation
[CH3:1][N:2]1[C:6]([C:7]2[CH:12]=[CH:11][CH:10]=[CH:9][CH:8]=2)=[N:5][N:4]=[C:3]1[SH:13].[Cl:14][CH2:15][CH2:16][CH2:17][N:18]1[CH2:26][C:25]2[C:20](=[CH:21][CH:22]=[C:23]([C:27](=[O:30])[CH2:28][CH3:29])[CH:24]=2)[CH2:19]1>>[ClH:14].[CH3:1][N:2]1[C:6]([C:7]2[CH:12]=[CH:11][CH:10]=[CH:9][CH:8]=2)=[N:5][N:4]=[C:3]1[S:13][CH2:15][CH2:16][CH2:17][N:18]1[CH2:26][C:25]2[C:20](=[CH:21][CH:22]=[C:23]([C:27](=[O:30])[CH2:28][CH3:29])[CH:24]=2)[CH2:19]1Participants
3
Procedure
The title compound was prepared in analogy to method 1.5 from 4-methyl-5-phenyl-4H-1,2,4-triazole-3-thiol (1.43 mmol, 0.33 g) and 1-[2-(3-chloropropyl)-2,3-dihydro-1H-isoindol-5-yl]propan-1-one (1.43 mmol, 0.36 g; preparation in analogy to 1.4 from isoindoline as disclosed in WO 0125200). Yield: 0.24 g.
Sources & evidence
- ORD record
- ord-4f98ff41258545dd9b10a2f3000168e7
- Source dataset
- uspto-grants-2008_12
- Patent number
- US07465744B2
Reaction notes
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