66686-30-4 → HCID 21510021, compound

HRID 1576964Notes

Reaction equation

HRID 1576964 reaction equation
CN(C)CCCCC(C1C=CC2C3C(=CC(C(=O)CCCCN(C)C)=CC=3)CC=2C=1)=O.[CH2:32]([N:34]([CH2:63][CH3:64])[CH2:35][CH2:36][CH2:37][C:38]([C:40]1[CH:52]=[CH:51][C:50]2[C:49]3[C:44](=[CH:45][C:46]([C:53](=[O:62])[CH2:54][CH2:55][CH2:56][N:57]([CH2:60][CH3:61])[CH2:58][CH3:59])=[CH:47][CH:48]=3)[CH2:43][C:42]=2[CH:41]=1)=[O:39])[CH3:33].[CH2:65]([N:67]([CH2:70][C:71]([C:73]1[CH:85]=[CH:84][C:83]2[C:82]3[C:77](=[CH:78][C:79]([C:86](=[O:93])[CH2:87][N:88]([CH2:91][CH3:92])[CH2:89][CH3:90])=[CH:80][CH:81]=3)[CH2:76][C:75]=2[CH:74]=1)=[O:72])[CH2:68][CH3:69])[CH3:66].N1(CCCC(C2C=CC3C4C(=CC(C(=O)CCCN5CCCCC5)=CC=4)CC=3C=2)=O)CCCCC1>>[CH2:60]([N:57]([CH2:58][CH3:59])[CH2:56][CH2:55][CH2:54][CH:53]([C:46]1[CH:47]=[CH:48][C:49]2[C:50]3[C:42](=[CH:41][C:40]([CH:38]([CH2:37][CH2:36][CH2:35][N:34]([CH2:32][CH3:33])[CH2:63][CH3:64])[OH:39])=[CH:52][CH:51]=3)[CH2:43][C:44]=2[CH:45]=1)[OH:62])[CH3:61].[CH2:91]([N:88]([CH2:87][CH:86]([C:79]1[CH:80]=[CH:81][C:82]2[C:83]3[C:75](=[CH:74][C:73]([CH:71]([CH2:70][N:67]([CH2:65][CH3:66])[CH2:68][CH3:69])[OH:72])=[CH:85][CH:84]=3)[CH2:76][C:77]=2[CH:78]=1)[OH:93])[CH2:89][CH3:90])[CH3:92]

Participants

6

Reactant 4

HCID 4798466686-30-4HCID 1602411,1'-(9H-Fluorene-2,7-diyl)bis(4-(1-piperidinyl)-1-butanone)HCID 515303HCID 515303, compoundHCID 515308HCID 515308, compound

Product 2

HCID 21510021HCID 21510021, compoundHCID 54499179HCID 54499179, compound

Procedure

Following essentially the same procedure but substituting the appropriate molar equivalent amounts of 2,7-bis(5-dimethylaminovaleryl)fluorene, 2,7-bis(4-diethylaminobutyryl)fluorene and 2,7-bis(diethylaminoacetyl)fluorene for the 2,7-bis(4-piperidinobutyryl) fluorene used as a starting material above, results in the formation of α,α'-bis(4-dimethylaminobutyl)-2,7-fluroenedimethanol, α,α'-bis(3-diethylaminopropyl)-2,7-fluorenedimethanol and α,α'-bis(diethylaminomethyl) 2,7-fluorenedimethanol, respectively.

Sources & evidence

ORD record
ord-da0764cc4288404a80c7022d270fce4d
Source dataset
uspto-grants-1976_09
Patent number
US03983124

Reaction notes

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