(4-Amino-3-nitrophenyl)-4-methylphenyl sulfoxide → HCID 67932468, compound

HRID 1762348Notes

Reaction equation

HRID 1762348 reaction equation
NC1C=CC(C2C=C(C)C=CC=2S(C2C=CC(C)=CC=2C2C=CC(N)=C([N+]([O-])=O)C=2)=O)=CC=1[N+]([O-])=O.[NH2:37][C:38]1[CH:43]=[CH:42][C:41]([C:44]2[C:48]([CH3:49])=[CH:47][S:46][C:45]=2[S:50]([C:52]2[S:53][CH:54]=[C:55]([CH3:67])[C:56]=2[C:57]2[CH:62]=[CH:61][C:60]([NH2:63])=[C:59]([N+:64]([O-])=O)[CH:58]=2)=[O:51])=[CH:40][C:39]=1[N+:68]([O-])=O>>[NH2:64][C:59]1[CH:58]=[C:57]([C:56]2[C:55]([CH3:67])=[CH:54][S:53][C:52]=2[S:50]([C:45]2[S:46][CH:47]=[C:48]([CH3:49])[C:44]=2[C:41]2[CH:42]=[CH:43][C:38]([NH2:37])=[C:39]([NH2:68])[CH:40]=2)=[O:51])[CH:62]=[CH:61][C:60]=1[NH2:63]

Participants

3

Reactant 2

HCID 53642139(4-Amino-3-nitrophenyl)-4-methylphenyl sulfoxideHCID 86741907HCID 86741907, compound

Product 1

HCID 67932468HCID 67932468, compound

Procedure

Following the procedure described in Example 40 but using as a starting material instead of (4-amino-3-nitrophenyl)-4-methylphenyl sulfoxide a corresponding amount of (4-amino-3-nitrophenyl)-4-methylthiophenyl sulfoxide, the title compound is obtained.

Sources & evidence

ORD record
ord-0d80a77ba55d49e6a5f8712eefd0b8d3
Source dataset
uspto-grants-1989_05
Patent number
US04831194

Reaction notes

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