(1E)-N'-Hydroxy-3-methoxypropanimidamide hydrochloride → HCID 58002514, compound
Reaction equation
[CH3:1][O:2][CH2:3][CH2:4][NH:5][C:6]([N:8]1[CH2:13][CH:12]([C:14]2[CH:19]=[CH:18][C:17]([C:20]([F:23])([F:22])[F:21])=[CH:16][CH:15]=2)[CH2:11][CH:10]([C:24]([OH:26])=O)[CH2:9]1)=[O:7].O[N:28]=[C:29]([NH2:34])[CH2:30][CH2:31][O:32][CH3:33]>>[CH3:1][O:2][CH2:3][CH2:4][NH:5][C:6]([N:8]1[CH2:13][CH:12]([C:14]2[CH:15]=[CH:16][C:17]([C:20]([F:21])([F:22])[F:23])=[CH:18][CH:19]=2)[CH2:11][CH:10]([C:24]2[O:26][N:34]=[C:29]([CH2:30][CH2:31][O:32][CH3:33])[N:28]=2)[CH2:9]1)=[O:7]Participants
3
Procedure
100 mg (0.267 mmol) of the compound from Example 105A and 78 mg (0.497 mmol) of N′-hydroxy-3-methoxypropanimidamide were reacted according to the General Method 2. Yield: 22 mg (17% of theory)
Sources & evidence
- ORD record
- ord-810c7e5869cf4772808aa32358adeb0a
- Source dataset
- uspto-grants-2012_02
- Patent number
- US08119663B2
Reaction notes
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