HCID 178422047, compound → HCID 178422049, compound

HRID 1425476Notes

Reaction equation

HRID 1425476 reaction equation
ClC1C=C2C(C)(C)/C(=C\C=C(/C3C=CC=C(CCCCC(O[N:70]4[C:74](=[O:75])[CH2:73][CH2:72][C:71]4=[O:76])=O)C=3)\C=C\C3C(C)(C)C4C5C=C(S([O-])(=O)=O)C=C(S([O-])(=O)=O)C=5C=CC=4[N+]=3CCCCS([O-])(=O)=O)/N=C2N(CCCCS([O-])(=O)=O)C=1.[Na+:77].[Na+].[Na+].[C:80]([CH2:83][CH2:84][C:85]1[CH:86]=[C:87](/[C:91](=[CH:125]\[CH:126]=[C:127]2/[C:128]([CH3:146])([CH3:145])[C:129]3[C:130](=[N:144]/2)[N:131]([CH2:136][CH2:137][CH2:138][CH2:139][S:140]([O-:143])(=[O:142])=[O:141])[CH:132]=[C:133]([Cl:135])[CH:134]=3)/[CH:92]=[CH:93]/[C:94]2[C:102]([CH3:104])([CH3:103])[C:101]3[C:100]4[CH:105]=[C:106]([S:113]([O-:116])(=[O:115])=[O:114])[CH:107]=[C:108]([S:109]([O-:112])(=[O:111])=[O:110])[C:99]=4[CH:98]=[CH:97][C:96]=3[N+:95]=2[CH2:117][CH2:118][CH2:119][CH2:120][S:121]([O-:124])(=[O:123])=[O:122])[CH:88]=[CH:89][CH:90]=1)([OH:82])=[O:81].[Na+].[Na+].[Na+]>>[Cl:135][C:133]1[CH:134]=[C:129]2[C:128]([CH3:146])([CH3:145])/[C:127](=[CH:126]\[CH:125]=[C:91](/[C:87]3[CH:88]=[CH:89][CH:90]=[C:85]([CH2:84][CH2:83][C:80]([O:82][N:70]4[C:74](=[O:75])[CH2:73][CH2:72][C:71]4=[O:76])=[O:81])[CH:86]=3)\[CH:92]=[CH:93]\[C:94]3[C:102]([CH3:103])([CH3:104])[C:101]4[C:100]5[CH:105]=[C:106]([S:113]([O-:116])(=[O:114])=[O:115])[CH:107]=[C:108]([S:109]([O-:112])(=[O:110])=[O:111])[C:99]=5[CH:98]=[CH:97][C:96]=4[N+:95]=3[CH2:117][CH2:118][CH2:119][CH2:120][S:121]([O-:124])(=[O:123])=[O:122])/[N:144]=[C:130]2[N:131]([CH2:136][CH2:137][CH2:138][CH2:139][S:140]([O-:143])(=[O:142])=[O:141])[CH:132]=1.[Na+:77].[Na+:77].[Na+:77]

Participants

3

Procedure

Compound 31 is prepared analogously to compound 29 (Example 38), except that compound 30 is used as a starting material.

Sources & evidence

ORD record
ord-e49928e8f476457895f73c51cab04a17
Source dataset
uspto-grants-2015_01
Patent number
US08927719B2

Reaction notes

Loading…