Isopropylamine → HCID 22768899, compound
Reaction equation
[O:1]1[CH2:29][CH:2]1[CH2:3][O:4][C:5]1[CH:10]=[CH:9][C:8]([S:11]([C:14]2[O:15][C:16]3[CH:28]=[CH:27][CH:26]=[CH:25][C:17]=3[C:18]=2[C:19]2[CH:24]=[CH:23][CH:22]=[CH:21][CH:20]=2)(=[O:13])=[O:12])=[CH:7][CH:6]=1.[CH:30]([NH2:33])([CH3:32])[CH3:31]>>[OH:1][CH:2]([CH2:29][NH:33][CH:30]([CH3:32])[CH3:31])[CH2:3][O:4][C:5]1[CH:6]=[CH:7][C:8]([S:11]([C:14]2[O:15][C:16]3[CH:28]=[CH:27][CH:26]=[CH:25][C:17]=3[C:18]=2[C:19]2[CH:20]=[CH:21][CH:22]=[CH:23][CH:24]=2)(=[O:13])=[O:12])=[CH:9][CH:10]=1Participants
3
Procedure
Treatment of 2-[(4-(2,3-epoxypropoxy)phenylsulfonyl]-3-phenylbenzofuran with isopropylamine as described in Example 3 gives the title compound.
Sources & evidence
- ORD record
- ord-650360001254448d858e5bb5046f6064
- Source dataset
- uspto-grants-1978_09
- Patent number
- US04117128
Reaction notes
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