HCID 54317093, compound → HCID 13987623, compound

HRID 256188Notes

Reaction equation

HRID 256188 reaction equation
[C:1]([N:9]1[CH2:14][CH2:13][N:12]([C:15]2[CH:20]=[CH:19][C:18]([N+:21]([O-])=O)=[C:17]([CH:24]=[C:25]3[NH:29][C:28](=[O:30])[NH:27][C:26]3=O)[CH:16]=2)[CH2:11][CH2:10]1)(=[O:8])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1>CO>[C:1]([N:9]1[CH2:14][CH2:13][N:12]([C:15]2[CH:20]=[CH:19][C:18]3[N:21]=[C:26]4[NH:27][C:28](=[O:30])[NH:29][C:25]4=[CH:24][C:17]=3[CH:16]=2)[CH2:11][CH2:10]1)(=[O:8])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1

Participants

3

Reactant 1

HCID 54317093HCID 54317093, compound

Product 1

HCID 13987623HCID 13987623, compound

Reagents, catalysts & solvents 1

HCID 887MethanolSolvent

Procedure

This compound, m.p. >300° C. (obtained as a methanol solvate by crystallization from dimethylformamidemethanol), was prepared analogous to Example 4 from 1-benzoyl-4-[3-[(2,4-dioxoimidazolidin-5-ylidene)methyl]-4-nitrophenyl)piperazine.

Sources & evidence

ORD record
ord-dc836fb7c6f1400aa40397d014496726
Source dataset
uspto-grants-1987_10
Patent number
US04701459

Reaction notes

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