Ethyl 3-hydrazino-3-oxopropionate → HCID 58002289, compound
Reaction equation
[N:1]1([C:7]([N:9]2[CH2:14][CH:13]([C:15]3[CH:20]=[CH:19][C:18]([O:21][C:22]([F:25])([F:24])[F:23])=[CH:17][CH:16]=3)[CH2:12][CH:11]([C:26](O)=O)[CH2:10]2)=[O:8])[CH2:6][CH2:5][O:4][CH2:3][CH2:2]1.[NH:29]([C:31](=[O:38])[CH2:32][C:33]([O:35][CH2:36][CH3:37])=[O:34])[NH2:30]>>[N:1]1([C:7]([N:9]2[CH2:14][CH:13]([C:15]3[CH:20]=[CH:19][C:18]([O:21][C:22]([F:25])([F:23])[F:24])=[CH:17][CH:16]=3)[CH2:12][CH:11]([C:26]3[O:38][C:31]([CH2:32][C:33]([O:35][CH2:36][CH3:37])=[O:34])=[N:29][N:30]=3)[CH2:10]2)=[O:8])[CH2:6][CH2:5][O:4][CH2:3][CH2:2]1Participants
3
Procedure
100 mg (0.249 mmol) of the compound from Example 44A and 40 mg (0.273 mmol) of ethyl 3-hydrazinyl-3-oxopropanoate were reacted according to the General Method 4. Yield: 9 mg (6% of theory).
Sources & evidence
- ORD record
- ord-b1f97507044f440db3a8370ba4d327d6
- Source dataset
- uspto-grants-2012_02
- Patent number
- US08119663B2
Reaction notes
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