Hydroxyamine hydrochloride → HCID 18654051, compound
Reaction equation
[CH3:1][O:2][C:3]1([C:9]2[S:13][C:12]([S:14][C:15]3[CH:20]=[CH:19][C:18]([C:21](=O)[CH3:22])=[CH:17][CH:16]=3)=[N:11][CH:10]=2)[CH2:8][CH2:7][O:6][CH2:5][CH2:4]1.Cl.[NH2:25][OH:26]>>[CH3:1][O:2][C:3]1([C:9]2[S:13][C:12]([S:14][C:15]3[CH:20]=[CH:19][C:18](/[C:21](=[N:25]/[OH:26])/[CH3:22])=[CH:17][CH:16]=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-ylthio]acetophenone was reacted with hydroxylamine hydrochloride to give (E)-4'-[5-(4-methoxytetrahydropyran-4-yl)thiazol-2-ylthio]acetophenone oxime in 80% yield, m.p. 114°-116° C.;
Sources & evidence
- ORD record
- ord-d09b5a593eef4a488c3e14d0a1eba707
- Source dataset
- uspto-grants-1996_01
- Patent number
- US05482966
Reaction notes
Loading…