Ethyl Acetoacetate → HCID 66745909, compound
Reaction equation
[NH2:1][C:2]1[C:3]([C:21]#[N:22])=[C:4]([CH:18]=[CH:19][CH:20]=1)[O:5][CH:6]1[CH2:11][CH2:10][CH:9]([NH:12][C:13](=[O:17])[CH:14]([CH3:16])[CH3:15])[CH2:8][CH2:7]1.O=[C:24]([CH3:31])[CH2:25][C:26]([O:28][CH2:29][CH3:30])=[O:27]>>[NH2:22][C:21]1[C:3]2[C:2](=[CH:20][CH:19]=[CH:18][C:4]=2[O:5][CH:6]2[CH2:7][CH2:8][CH:9]([NH:12][C:13](=[O:17])[CH:14]([CH3:16])[CH3:15])[CH2:10][CH2:11]2)[N:1]=[C:24]([CH3:31])[C:25]=1[C:26]([O:28][CH2:29][CH3:30])=[O:27]Participants
3
Procedure
Prepared as in Example 2a from N-(4-(3-amino-2-cyanophenoxy)cyclohexyl)isobutyramide (Example 40b) and ethyl 3-oxobutanoate as a yellow solid (57%). MS 414 (MH+).
Sources & evidence
- ORD record
- ord-1ade1266753d474bb4b7fe2e04e65fa2
- Source dataset
- uspto-grants-2015_06
- Patent number
- US09049878B2
Reaction notes
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