HCID 42610890, compound → HCID 178450457, compound

HRID 1021148Notes

Reaction equation

HRID 1021148 reaction equation
[NH2:1][CH2:2][C:3]1[CH:4]=[C:5]([CH:16]=[CH:17][CH:18]=1)[CH2:6][CH2:7][C:8]([OH:15])([CH2:12][CH2:13][CH3:14])[CH2:9][CH2:10][CH3:11].N1([CH:24]([NH:29][C:30](=[O:36])[O:31][C:32]([CH3:35])([CH3:34])[CH3:33])[NH:25][C:26](=[O:28])[O-:27])C=CC=N1>CC#N>[C:32]([O:31][C:30](=[O:36])[N:29]=[C:24]([NH:25][C:26]([O:27][C:3]([CH3:4])([CH3:18])[CH3:2])=[O:28])[NH:1][CH2:2][C:3]1[CH:18]=[CH:17][CH:16]=[C:5]([CH2:6][CH2:7][C:8]([OH:15])([CH2:9][CH2:10][CH3:11])[CH2:12][CH2:13][CH3:14])[CH:4]=1)([CH3:33])([CH3:34])[CH3:35]

Participants

4

Reactant 2

HCID 42610890HCID 42610890, compoundHCID 86635872HCID 86635872, compound

Product 1

HCID 178450457HCID 178450457, compound

Reagents, catalysts & solvents 1

HCID 6342AcetonitrileSolvent

Procedure

Reaction of 4-(3-(aminomethyl)phenethyl)heptan-4-ol with tert-butyl (1H-pyrazol-1-yl)methylenedicarbamate in CH3CN gives tert-butyl(tert-butoxycarbonylamino)(3-(3-hydroxy-3-propylhexyl)benzylamino)methylenecarbamate.

Sources & evidence

ORD record
ord-956e6c50b96f4dbaa370b7498e500069
Source dataset
uspto-grants-2014_05
Patent number
US08716529B2

Reaction notes

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