N-[[2-chloro-3-(phenyliminomethyl)cyclohex-2-en-1-ylidene]methyl]aniline;hydrochloride → HCID 178422058, compound

HRID 1480509Notes

Reaction equation

HRID 1480509 reaction equation
Br/C(/C=C/C1C(C)(C)C2C(N=1)=[N+](CCCS([O-])(=O)=O)C=C(Cl)C=2)=C\C=C1\N(CCCS([O-])(=O)=O)C2C(C\1(C)C)=CC(S([O-])(=O)=O)=CC=2.[Na+:48].[Na+].[CH3:50][C:51]1[C:59]([CH3:61])([CH3:60])[C:58]2[C:53](=[CH:54][CH:55]=[C:56]([S:62]([O-:65])(=[O:64])=[O:63])[CH:57]=2)[N+:52]=1[CH2:66][CH2:67][CH2:68][S:69]([O-:72])(=[O:71])=[O:70].[Na+].[CH3:74][C:75]1[C:76]([CH3:92])([CH3:91])[C:77]2[C:78]([N:90]=1)=[N+:79]([CH2:83][CH2:84][CH2:85][S:86]([O-:89])(=[O:88])=[O:87])[CH:80]=[CH:81][CH:82]=2.Cl.N([CH:101]=[C:102]1[CH2:107][CH2:106][CH2:105][C:104]([CH:108]=NC2C=CC=CC=2)=[C:103]1[Cl:116])C1C=CC=CC=1>>[Cl:116][C:103]1=[C:104]([CH:108]=[CH:50][C:51]2[C:59]([CH3:60])([CH3:61])[C:58]3[C:53](=[CH:54][CH:55]=[C:56]([S:62]([O-:65])(=[O:64])=[O:63])[CH:57]=3)[N+:52]=2[CH2:66][CH2:67][CH2:68][S:69]([O-:72])(=[O:71])=[O:70])[CH2:105][CH2:106][CH2:107]/[C:102]/1=[CH:101]\[CH:74]=[C:75]1/[C:76]([CH3:92])([CH3:91])[C:77]2[C:78](=[N:90]/1)[N:79]([CH2:83][CH2:84][CH2:85][S:86]([O-:89])(=[O:88])=[O:87])[CH:80]=[CH:81][CH:82]=2.[Na+:48].[Na+:48]

Participants

5

Reactant 4

HCID 53399086N-[[2-chloro-3-(phenyliminomethyl)cyclohex-2-en-1-ylidene]methyl]aniline;hydrochlorideHCID 577633353-(2,3,3-Trimethyl-3H-pyrrolo[2,3-b]pyridin-7-ium-7-yl)propane-1-sulfonateHCID 71692790HCID 71692790, compoundHCID 86699468HCID 86699468, compound

Product 1

HCID 178422058HCID 178422058, compound

Procedure

Compound 16 is prepared analogously to compound 9 (Example 9), except that compound 4, compound 7, and N-[(3-(anilinomethylene)-2-chloro-1-cyclohexen-1-yl)methylene]aniline monohydrochloride are used as starting materials.

Sources & evidence

ORD record
ord-1467c237af9742f1a78234f99beded96
Source dataset
uspto-grants-2016_08
Patent number
US09408924B2

Reaction notes

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