Reaction equation
[ClH:1].Cl.[OH:3][NH:4][C:5]([NH:17][CH3:18])=[N:6][CH2:7][CH2:8][S:9][CH2:10][C:11]1[NH:15][CH:14]=[N:13][C:12]=1[CH3:16].[CH2:19](ON)[C:20]1[CH:25]=[CH:24][CH:23]=[CH:22][CH:21]=1.Cl.Cl.Cl.ON(CCSCC1NC=NC=1C)C(N)=NCCSCC1NC=NC=1C>>[ClH:1].[ClH:1].[CH3:18][NH:17][C:5]([NH:4][O:3][CH2:19][C:20]1[CH:25]=[CH:24][CH:23]=[CH:22][CH:21]=1)=[N:6][CH2:7][CH2:8][S:9][CH2:10][C:11]1[NH:15][CH:14]=[N:13][C:12]=1[CH3:16]Participants
4
Procedure
Reaction of the isothiourea dihydrochloride of Example 1 (i) with benzyloxyamine by the procedure of Example 1 (ii) gave the title product.
Sources & evidence
- ORD record
- ord-a75f914148014f11b312ab851651fbf8
- Source dataset
- uspto-grants-1977_07
- Patent number
- US04034101
Linked notes
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