3,5-Diamino-1,2,4-triazole → HCID 66842429, compound
Reaction equation
[Cl:1][C:2]1[CH:7]=[CH:6][C:5]([S:8]([N:11]2[CH:16]3[CH2:17][CH2:18][CH2:19][CH:12]2[C:13](=[CH:21]O)[C:14](=O)[CH2:15]3)(=[O:10])=[O:9])=[CH:4][CH:3]=1.[NH2:23][C:24]1[N:28]=[C:27]([NH2:29])[NH:26][N:25]=1>>[Cl:1][C:2]1[CH:7]=[CH:6][C:5]([S:8]([N:11]2[CH:16]3[CH2:17][CH2:18][CH2:19][CH:12]2[C:13]2[CH:21]=[N:23][C:24]4[N:25]([C:14]=2[CH2:15]3)[N:26]=[C:27]([NH2:29])[N:28]=4)(=[O:10])=[O:9])=[CH:4][CH:3]=1Participants
3
Procedure
Prepared as described in Example 5 using 9-(4-chlorophenylsulfonyl)-2-(hydroxymethylene)-9-azabicyclo[3.3.1]nonan-3-one which was prepared as described in Example 34 and 3,5-diamino-1,2,4-triazole.
Workup
- customPrepared
- customwas prepared
Sources & evidence
- ORD record
- ord-7fd5f63e4ce440b889e7aa21dd6a0f98
- Source dataset
- uspto-grants-2008_03
- Patent number
- US07345056B2
Reaction notes
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