Isopropylamine → HCID 11221952, compound
Reaction equation
CC1C=CC(S(O[CH2:12][CH:13]2[CH2:17][C:16]3[CH:18]=[C:19]([F:30])[CH:20]=[C:21]([C:22]4[C:27]([Cl:28])=[CH:26][CH:25]=[CH:24][C:23]=4[Cl:29])[C:15]=3[O:14]2)(=O)=O)=CC=1.[CH:31]([NH2:34])([CH3:33])[CH3:32]>>[Cl:29][C:23]1[CH:24]=[CH:25][CH:26]=[C:27]([Cl:28])[C:22]=1[C:21]1[C:15]2[O:14][CH:13]([CH2:12][NH:34][CH:31]([CH3:33])[CH3:32])[CH2:17][C:16]=2[CH:18]=[C:19]([F:30])[CH:20]=1Participants
3
Procedure
The title compound was prepared (0.065 g, 66%) following the general procedure of Example 390 as a white solid, hydrochloride salt from (±)-([5-fluoro-7-(2,6-dichlorophenyl)-2,3-dihydro-1-benzofuran-2-yl]methyl 4-methylbenzenesulfonate (0.14 g, 0.3 mmol) and isopropylamine (0.18 g, 3.0 mmol). mp 134-135° C.
Sources & evidence
- ORD record
- ord-4b176942298a48728ae0fe6a3e9d1594
- Source dataset
- uspto-grants-2008_10
- Patent number
- US07435837B2
Reaction notes
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