HCID 42610457, compound → HCID 178450456, compound

HRID 1021149Notes

Reaction equation

HRID 1021149 reaction equation
[NH2:1][CH2:2][CH2:3][CH2:4][C:5]1[CH:6]=[C:7]([CH:18]=[CH:19][CH:20]=1)[CH2:8][CH2:9][C:10]([OH:17])([CH2:14][CH2:15][CH3:16])[CH2:11][CH2:12][CH3:13].N1([CH:26]([NH:31][C:32](=[O:38])[O:33][C:34]([CH3:37])([CH3:36])[CH3:35])[NH:27][C:28](=[O:30])[O-:29])C=CC=N1>>[C:34]([O:33][C:32](=[O:38])[N:31]=[C:26]([NH:27][C:28]([O:29][C:5]([CH3:6])([CH3:20])[CH3:4])=[O:30])[NH:1][CH2:2][CH2:3][CH2:4][C:5]1[CH:20]=[CH:19][CH:18]=[C:7]([CH2:8][CH2:9][C:10]([OH:17])([CH2:11][CH2:12][CH3:13])[CH2:14][CH2:15][CH3:16])[CH:6]=1)([CH3:35])([CH3:36])[CH3:37]

Participants

3

Reactant 2

HCID 42610457HCID 42610457, compoundHCID 86635872HCID 86635872, compound

Product 1

HCID 178450456HCID 178450456, compound

Procedure

Reaction of 4-(3-(3-aminopropyl)phenethyl)heptan-4-ol with tert-butyl (1H-pyrazol-1-yl)methylenedicarbamate following the method described in Example 168 gives tert-butyl(tert-butoxycarbonylamino)(3-(3-(3-hydroxy-3-propylhexyl)phenyl)propylamino)methylenecarbamate.

Sources & evidence

ORD record
ord-8fa6a111dbc24e05891cdce8ec9cf375
Source dataset
uspto-grants-2014_05
Patent number
US08716529B2

Reaction notes

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