Bis(2-amino-1H-imidazole) sulphate → HCID 66842412, 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.S(O)(O)(=O)=O.[NH2:28][C:29]1[NH:30][CH:31]=[CH:32][N:33]=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:28][C:29]4[N:33]([C:14]=2[CH2:15]3)[CH:32]=[CH:31][N:30]=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 2-aminoimidazole sulfate.
Workup
- customPrepared
- customwas prepared
Sources & evidence
- ORD record
- ord-d746a195d4ba4b06aa3c0c41714a79a5
- Source dataset
- uspto-grants-2010_07
- Patent number
- US07754712B2
Reaction notes
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