Hydroxyamine hydrochloride → HCID 18654050, compound
Reaction equation
[CH3:1][O:2][C:3]1([C:9]2[S:13][C:12]([O:14][CH2:15][C:16]3[CH:21]=[CH:20][C:19]([C:22](=O)[CH3:23])=[CH:18][CH:17]=3)=[N:11][CH:10]=2)[CH2:8][CH2:7][O:6][CH2:5][CH2:4]1.Cl.[NH2:26][OH:27]>>[CH3:1][O:2][C:3]1([C:9]2[S:13][C:12]([O:14][CH2:15][C:16]3[CH:21]=[CH:20][C:19](/[C:22](=[N:26]/[OH:27])/[CH3:23])=[CH:18][CH:17]=3)=[N:11][CH:10]=2)[CH2:8][CH2:7][O:6][CH2:5][CH2:4]1Participants
3
Procedure
Using an analogous procedure to that described in Example 15, 4'-[5-(4-methoxytetrahydropyran-4-yl)thiazol-2-yloxymethyl]acetophenone was reacted with hydroxylamine hydrochloride to give (E)-4'-[5-(4-methoxytetrahydropyran-4-yl)thiazol-2-yloxymethyl]acetophenone oxime in 57% yield, m.p. 107°-109° C.;
Sources & evidence
- ORD record
- ord-b1a29a40a1ed46bdacb7415f2fc2a112
- Source dataset
- uspto-grants-1996_01
- Patent number
- US05482966
Reaction notes
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