Hydrazinecarboxaldehyde → HCID 68954223, compound
Reaction equation
[C:1]([NH:4][NH:5][C:6](=[O:26])[CH2:7][N:8]1[C:12]([CH2:13][CH3:14])=[C:11]([O:15][C:16]2[CH:21]=[CH:20][C:19]([C:22]#[N:23])=[CH:18][CH:17]=2)[C:10]([CH2:24][CH3:25])=[N:9]1)(=[O:3])C.C(C1C=CC(OC2C(CC)=NN(CC(O)=O)C=2CC)=CC=1)#N.C(NN)=O>>[C:22]([C:19]1[CH:18]=[CH:17][C:16]([O:15][C:11]2[C:10]([CH2:24][CH3:25])=[N:9][N:8]([CH2:7][C:6]([NH:5][NH:4][CH:1]=[O:3])=[O:26])[C:12]=2[CH2:13][CH3:14])=[CH:21][CH:20]=1)#[N:23]Participants
4
Procedure
The title compound (290 mg, 51%) was prepared by a similar method to that describe for the acetohydrazide of step (b) of Example 140 using the acid of step (a) of Example 140 and formic hydrazide as the starting materials.
Sources & evidence
- ORD record
- ord-3c3b1f7eab8c4ba29926da2b538866be
- Source dataset
- uspto-grants-2009_01
- Patent number
- US07482375B2
Reaction notes
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