HCID 18358094, compound → HCID 18358210, compound

HRID 428298Notes

Reaction equation

HRID 428298 reaction equation
[C:1]([O:5][C:6]1[CH:29]=[CH:28][CH:27]=[CH:26][C:7]=1[C:8]([C:10]1[CH:15]=[CH:14][C:13]([NH:16][C:17]2[CH:22]=[CH:21][CH:20]=[CH:19][C:18]=2[N+:23]([O-])=O)=[CH:12][CH:11]=1)=[O:9])([CH3:4])([CH3:3])[CH3:2].COC1C=C(NC2C=CC=CC=2[N+]([O-])=O)C=CC=1C(C1C=CC=CC=1C)=O>>[NH2:23][C:18]1[CH:19]=[CH:20][CH:21]=[CH:22][C:17]=1[NH:16][C:13]1[CH:14]=[CH:15][C:10]([C:8]([C:7]2[CH:26]=[CH:27][CH:28]=[CH:29][C:6]=2[O:5][C:1]([CH3:2])([CH3:3])[CH3:4])=[O:9])=[CH:11][CH:12]=1

Participants

3

Reactant 2

HCID 18358094HCID 18358094, compound2×HCID 18358116HCID 18358116, compound

Product 1

HCID 18358210HCID 18358210, compound

Procedure

By following the procedure of example 70, but using 2-tert-butoxy-4′-(2-nitrophenylamino)benzophenone (Compound 256) in place of 2-methoxy-2′-methyl-4-(2-nitrophenylamino)benzophenone (Compound 255), the desired compound was obtained.

Sources & evidence

ORD record
ord-502c96661fe14d498cbbb59ba5b6f02d
Source dataset
uspto-grants-2001_11
Patent number
US06313174B1

Reaction notes

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