Hydroxyamine hydrochloride → HCID 18996065, compound
Reaction equation
[CH3:1][O:2][C:3]1([C:9]2[CH:10]=[C:11]([S:14][C:15]3[CH:24]=[C:23]4[C:18]([C:19](=O)[CH2:20][CH2:21][O:22]4)=[CH:17][CH:16]=3)[S:12][CH:13]=2)[CH2:8][CH2:7][O:6][CH2:5][CH2:4]1.Cl.[NH2:27][OH:28]>>[CH3:1][O:2][C:3]1([C:9]2[CH:10]=[C:11]([S:14][C:15]3[CH:24]=[C:23]4[C:18](/[C:19](=[N:27]/[OH:28])/[CH2:20][CH2:21][O:22]4)=[CH:17][CH:16]=3)[S:12][CH:13]=2)[CH2:8][CH2:7][O:6][CH2:5][CH2:4]1Participants
3
Procedure
Using an analogous procedure to that described in Example 7, 7-[4-(4-methoxytetrahydropyran-4-yl)thien-2-ylthio]chroman-4-one was reacted with hydroxylamine hydrochloride to give (E)-7-[4-(4-methoxytetrahydropyran-4-yl)thien-2-ylthio]chroman-4-one oxime in 82% yield, m.p. 137°-138° C.;
Sources & evidence
- ORD record
- ord-d33a297f73ff4bfd850dae1c1795183e
- Source dataset
- uspto-grants-1996_01
- Patent number
- US05482966
Reaction notes
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