HCID 22459286, compound → HCID 22459287, compound

HRID 2185022Notes

Reaction equation

HRID 2185022 reaction equation
CC(N(C(C)C)CCOC1C=C(NC(=O)C2C=CC(C3[CH:29]=[CH:28][CH:27]=[CH:26][N:25]=3)=CC=2)C=CC=1OC)C.CC(N(C(C)C)CCOC1C=C(NC(=O)C2C=CC(C3SC=CN=3)=CC=2)C=CC=1OC)C.[CH3:66][CH:67]([N:69]([CH:96]([CH3:98])[CH3:97])[CH2:70][CH2:71][O:72][C:73]1[CH:74]=[C:75]([NH:81][C:82]([C:84]2[CH:85]=[N:86][C:87](C3C=CC=CC=3)=[CH:88][CH:89]=2)=[O:83])[CH:76]=[CH:77][C:78]=1[O:79][CH3:80])[CH3:68].CC(N(C(C)C)CCOC1C=C(NC(=O)C2C=CC(C3C=CN=CC=3)=CC=2)C=CC=1OC)C>>[CH3:98][CH:96]([N:69]([CH:67]([CH3:68])[CH3:66])[CH2:70][CH2:71][O:72][C:73]1[CH:74]=[C:75]([NH:81][C:82]([C:84]2[CH:85]=[N:86][CH:87]=[C:88]([N:25]3[CH:26]=[CH:27][CH:28]=[CH:29]3)[CH:89]=2)=[O:83])[CH:76]=[CH:77][C:78]=1[O:79][CH3:80])[CH3:97]

Participants

5

Reactant 4

HCID 22459286HCID 22459286, compoundHCID 22459310HCID 22459310, compoundHCID 22459339HCID 22459339, compoundHCID 22459341HCID 22459341, compound

Product 1

HCID 22459287HCID 22459287, compound

Procedure

N-[3-[2-[Bis(1-methylethyl)amino]ethoxy]-4-methoxyphenyl]-4-(2-pyridinyl)benzamide; N-[3-[2-[Bis(1-methylethyl)amino]ethoxy]-4-methoxyphenyl]-4-(2-thiazolyl)benzamide; N-[3-[2-[Bis(1-methylethyl)amino]ethoxy]-4-methoxyphenyl]-6-phenyl-3-pyridinecarboxamide; and N-[3-[2-[Bis(1-methylethyl)amino]ethoxy]-4-methoxyphenyl]-4-(4-pyridinyl)benzamide

Sources & evidence

ORD record
ord-74c75decd6604be183af9020fbbff0e7
Source dataset
uspto-grants-2002_06
Patent number
US06399656B1

Reaction notes

Loading…