Formamidine acetate → HCID 46884005, 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.C(O)(=O)C.[CH:27]([NH2:29])=[NH:28]>>[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][CH:27]=[N:29][C:14]=2[CH2:15]3)(=[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 formamidine acetate. See also: Hajos, Gyorgy; Snatzke, Guenther Liebigs Annalen der Chemie 1989, (1), 31-3.
Workup
- customPrepared
- customwas prepared
Sources & evidence
- ORD record
- ord-203a5ef5e2e4415fa24bf338f545be13
- Source dataset
- uspto-grants-2008_03
- Patent number
- US07345056B2
Reaction notes
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